Epilepsy and Brain Malformation

Analysis of all known genes associated with epilepsy and brain malformation

GC_23 Epilepsy

Epilepsy is a heterogeneous group of disorders characterized by recurrent unprovoked seizures, which may arise from genetic abnormalities affecting neuronal excitability, synaptic function, metabolism, or brain development. Genetic epilepsies range from isolated seizure disorders to severe developmental and epileptic encephalopathies.

This panel includes genes associated with a broad spectrum of genetic epilepsies, including channelopathies, synaptic disorders, metabolic and mitochondrial epilepsies, developmental and epileptic encephalopathies, and neurodevelopmental disorders in which epilepsy is a major feature.

This panel is recommended for patients with unexplained epilepsy of any age, particularly those with early-onset seizures, developmental and epileptic encephalopathy, developmental delay or intellectual disability, structural brain abnormalities, or additional neurologic or neurodevelopmental features.

Last update: 19.01.2026

AARS1, AASS, ABAT, ABCA2, ABCD1, ACOX1, ACTL6B, ACY1, ADAM22, ADAR, ADARB1, ADAT3, ADD1, ADGRG1, ADGRL1, ADNP, ADPRS, ADSL, AFF3, AFG3L2, AGA, AGO1, AIFM1, AIMP1, AIMP2, AJAP1, AKT3, ALDH3A2, ALDH5A1, ALDH7A1, ALG1, ALG11, ALG12, ALG13, ALG14, ALG3, ALG6, ALG8, ALG9, ALKBH8, ALPL, AMACR, AMPD2, AMT, ANK2, ANKRD11, ANO4, AP1G1, AP2M1, AP3B2, AP4B1, AP4E1, AP4M1, AP4S1, APC2, ARF1, ARF3, ARFGEF1, ARFGEF2, ARG1, ARHGEF15, ARHGEF9, ARID1B, ARSA, ARV1, ARX, ASAH1, ASH1L, ASL, ASNS, ASPA, ASXL3, ATAD1, ATN1, ATP13A2, ATP1A1, ATP1A2, ATP1A3, ATP2B1, ATP5F1A, ATP5PO, ATP6AP2, ATP6V0A1, ATP6V0A2, ATP6V0C, ATP6V1A, ATP7A, ATRX, BAIAP2, BAP1, BCKDHA, BCKDHB, BCKDK, BCS1L, BLOC1S1, BOLA3, BORCS8, BRAF, BRAT1, BRSK1, BSCL2, BSN, BTD, C12ORF57, C12orf57, C2orf69, CACNA1A, CACNA1B, CACNA1C, CACNA1D, CACNA1E, CACNA1G, CACNA1H, CACNA1I, CACNA2D1, CACNA2D2, CACNB4, CAD, CAMK2B, CAMK2D, CAMSAP1, CAPRIN1, CARS2, CASK, CASR, CC2D1A, CC2D2A, CCDC88A, CCDC88C, CDC42BPB, CDK19, CDK5, CDK9, CDKL5, CELF2, CELF4, CEP85L, CERS1, CERT1, CHD2, CHD4, CHD5, CHKA, CHRNA2, CHRNA4, CHRNB2, CIC, CILK1, CLCN2, CLCN3, CLCN4, CLCN6, CLDN5, CLN2 , CLN3, CLN5, CLN6, CLN8, CLPB, CLTC, CNKSR2, CNNM2, CNOT9, CNPY3, CNTN2, CNTNAP2, COA7, COA8, COG3, COG4, COG5, COG6, COG7, COG8, COL18A1, COL4A1, COL4A2, COLGALT1, COQ2, COQ4, COQ6, COQ9, COX10, COX11, COX15, COX6B1, CPA6, CPLX1, CPSF3, CPT2, CREBBP, CRELD1, CRNKL1, CRPPA, CSF1R, CSNK1G1, CSNK2B, CSTB, CTC1, CTNNA2, CTNNB1, CTSD, CTSF, CTU2, CUL3, CUL4B, CUX1, CUX2, CYFIP2, CYP27A1, D2HGDH, DALRD3, DARS1, DARS2, DBT, DCX, DDC, DDX3X, DEAF1, DEGS1, DENND5A, DENND5B, DEPDC5, DHCR24, DHCR7, DHDDS, DHFR, DHPS, DHRSX, DHX16, DHX30, DIAPH1, DLL1, DMXL2, DNAJC5, DNAJC6, DNM1, DNM1L, DOCK7, DOLK, DPAGT1, DPH5, DPM1, DPM2, DPYD, DPYS, DROSHA, DTYMK, DYNC1H1, DYRK1A, EARS2, ECHS1, ECM1, EEF1A2, EEFSEC, EFHC1, EFTUD2, EHMT1, EIF2AK2, EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5, EIF2S3, EIF3F, EIF4A2, ELFN1, EMC1, EMC10, EML1, EMX2, ENTPD1, EPB41L3, EPG5, EPM2A, EPRS1, ESAM, ETFA, ETFB, ETFDH, ETHE1, EXOC7, EXOSC3, EXT2, FA2H, FAM126A, FAM50A, FAR1, FARS2, FASTKD2, FBXL4, FBXO11, FBXO28, FCSK, FDFT1, FDX2, FGF12, FGF13, FGFR3, FH, FKRP, FKTN, FLNA, FOLR1, FOXG1, FOXP1, FOXRED1, FRMD5, FRRS1L, FUCA1, FUT8, FZR1, GABBR2, GABRA1, GABRA2, GABRA5, GABRB1, GABRB2, GABRB3, GABRD, GABRG2, GAD1, GALC, GALNT2, GAMT, GATAD2B, GATM, GCDH, GCH1, GCSH, GFAP, GFM1, GFM2, GJC2, GLB1, GLDC, GLI3, GLRA1, GLRA2, GLRB, GLS, GLUD1, GLUL, GLYCTK, GM2A, GNAO1, GNAQ, GNB1, GNB5, GNE, GOLGA2, GOSR2, GOT2, GPAA1, GPHN, GRIA2, GRIA3, GRIA4, GRIK2, GRIN1, GRIN2A, GRIN2B, GRIN2D, GRM7, GRN, GSS, GTF3C3, GTPBP2, GTPBP3, GUF1, H3-3A, H3-3B, HACE1, HAX1, HCCS, HCFC1, HCN1, HCN2, HDAC8, HEATR5B, HECTD4, HECW2, HEPACAM, HERC2, HEXA, HEXB, HIBCH, HID1, HLCS, HMGCL, HNRNPH2, HNRNPR, HNRNPU, HOXA1, HPDL, HPRT1, HRAS, HSD17B10, HSD17B4, HSPD1, HTRA1, HTRA2, IBA57, IER3IP1, IFIH1, IKBKG, INPP4A, IQSEC2, IRF2BPL, ITPA, JAKMIP1, JMJD1C, KARS1, KAT5, KAT8, KATNB1, KCNA1, KCNA2, KCNA3, KCNB1, KCNB2, KCNC1, KCNC2, KCND2, KCND3, KCNH1, KCNH2, KCNH5, KCNJ10, KCNJ11, KCNK4, KCNMA1, KCNQ2, KCNQ3, KCNQ5, KCNT1, KCNT2, KCTD3, KCTD7, KDM5C, KDM6B, KIAA1109, KICS2, KIF1A, KIF2A, KIF5A, KIF5C, KIFBP, KLHL20, KMT2E, KPNA7, KPTN, KRAS, L2HGDH, LAMC3, LARGE1, LARS1, LETM1, LGI1, LIAS, LIPT1, LIPT2, LMAN2L, LMBRD2, LMNB1, LMNB2, LNPK, LRPPRC, LRRC45, LSS, LYRM7, LYST, MACF1, MADD, MAF, MAGI2, MANBA, MAP2K1, MAP2K2, MARK2, MARS2, MAST1, MAST3, MAST4, MBD5, MBOAT7, MDH1, MDH2, MECP2, MED11, MED12, MED17, MED27, MEF2C, MFF, MFSD8, MICAL1, MINPP1, MIPEP, MLC1, MMACHC, MMADHC, MOCS1, MOCS2, MOCS3, MOGS, MPDU1, MRPL44, MT-ATP6, MT-ATP8, MT-CO1, MT-CO2, MT-CO3, MT-CYB, MT-ND1, MT-ND2, MT-ND3, MT-ND4, MT-ND4L, MT-ND5, MT-ND6, MT-RNR1, MT-RNR2, MT-TA, MT-TC, MT-TD, MT-TE, MT-TF, MT-TG, MT-TH, MT-TI, MT-TK, MT-TL1, MT-TL2, MT-TM, MT-TN, MT-TP, MT-TQ, MT-TR, MT-TS1, MT-TS2, MT-TT, MT-TV, MT-TW, MT-TY, MTFMT, MTHFR, MTHFS, MTOR, MTR, NACC1, NAGA, NAGLU, NAPB, NARS1, NARS2, NBEA, NCDN, NDE1, NDP, NDST1, NDUFA1, NDUFA10, NDUFA2, NDUFAF2, NDUFAF3, NDUFAF4, NDUFAF5, NDUFAF6, NDUFS1, NDUFS2, NDUFS4, NDUFS6, NDUFS7, NDUFS8, NDUFV1, NECAP1, NEDD4L, NEU1, NEUROD2, NEXMIF, NFU1, NGLY1, NHLRC1, NKX6-2, NOTCH3, NPC1, NPC2, NPRL2, NPRL3, NR2F1, NR4A2, NRROS, NRXN1, NSD1, NSDHL, NSF, NSRP1, NT5C2, NTRK2, NUBPL, NUP214, NUS1, OCLN, OFD1, OGDHL, OPHN1, OTUD6B, OTUD7A, OTX2, OXR1, P4HTM, PABPC1, PACS1, PACS2, PAFAH1B1, PAH, PAK1, PARP6, PARS2, PCCA, PCCB, PCDH12, PCDH19, PCDHGC4, PCLO, PCYT2, PDHA1, PDHX, PDSS2, PET100, PEX1, PEX10, PEX12, PEX13, PEX14, PEX16, PEX19, PEX2, PEX26, PEX3, PEX5, PEX6, PEX7, PGK1, PGM2L1, PHACTR1, PHF6, PHGDH, PI4K2A, PIDD1, PIGA, PIGB, PIGC, PIGG, PIGH, PIGK, PIGM, PIGN, PIGO, PIGP, PIGQ, PIGS, PIGT, PIGU, PIGV, PIGW, PIK3AP1, PIK3R2, PIP5K1C, PITRM1, PLA2G6, PLAA, PLCB1, PLK1, PLP1, PLPBP, PLXNA1, PMM2, PMPCB, PNKD, PNKP, PNPLA8, PNPO, PNPT1, POLG, POLG2, POLR3A, POLR3B, POMGNT1, POMT1, POMT2, PPFIBP1, PPIL1, PPOX, PPP1R3F, PPP2CA, PPP2R1A, PPP2R2B, PPP2R5C, PPP2R5D, PPP3CA, PPT1, PRDM8, PRICKLE1, PRICKLE2, PRIMA1, PRMT7, PRODH, PRPF8, PRRT2, PRUNE1, PSAP, PSAT1, PSPH, PTCD3, PTEN, PTF1A, PTPMT1, PTPN23, PTS, PUM1, PURA, PYCR2, QARS1, QDPR, RAB11A, RAB11B, RAB18, RAB39B, RAB3GAP1, RAB3GAP2, RAB5C, RAC3, RAI1, RALA, RALGAPA1, RANBP2, RARS1, RARS2, RBFOX1, RBFOX3, RELN, RFT1, RHEB, RHOBTB2, RMND1, RNASEH2A, RNASEH2B, RNASEH2C, RNASET2, RNF113A, RNF13, RNF2, RNF216, RNU2-2P, RNU4-2, RNU4ATAC, RNU5B-1, ROGDI, RORA, RORB, RPIA, RRM2B, RTN4IP1, RTTN, RUSC2, RYR2, RYR3, SAMD12, SAMHD1, SARS1, SATB1, SATB2, SCAF4, SCAMP5, SCARB2, SCN1A, SCN1B, SCN2A, SCN3A, SCN8A, SCO1, SCO2, SCP2, SDHA, SDHAF1, SEMA6B, SEPSECS, SERAC1, SERPINI1, SETBP1, SETD1A, SETD1B, SETD5, SGCE, SGSH, SHQ1, SIK1, SIX3, SLC12A5, SLC13A3, SLC13A5, SLC16A2, SLC19A3, SLC1A2, SLC1A4, SLC25A1, SLC25A12, SLC25A15, SLC25A22, SLC25A42, SLC2A1, SLC31A1, SLC32A1, SLC35A1, SLC35A2, SLC35A3, SLC38A3, SLC39A8, SLC45A1, SLC46A1, SLC4A10, SLC5A6, SLC6A1, SLC6A5, SLC6A8, SLC7A6OS, SLC9A6, SMARCA2, SMARCC2, SMC1A, SMS, SNAP25, SNF8, SNIP1, SNORD118, SNX27, SOX10, SPATA5, SPATA5L1, SPOUT1, SPR, SPTAN1, SPTBN1, SPTBN4, SRPX2, SSR4, ST3GAL3, ST3GAL5, STAG1, STAG2, STAMBP, STARD7, STRADA, STX1B, STXBP1, STXBP2, SUCLA2, SUCLG1, SUMF1, SUOX, SURF1, SV2A, SYN1, SYNCRIP, SYNGAP1, SYNJ1, SZT2, TAF1, TAF8, TANC2, TANGO2, TARS2, TBC1D20, TBC1D24, TBC1D2B, TBCD, TBCE, TBCK, TBL1XR1, TCF4, TDP2, TEFM, TELO2, TET3, TFE3, TH, TIAM1, TIMM50, TK2, TMEM106B, TMEM167A, TMEM222, TMEM63B, TMEM70, TMX2, TNK2, TNPO2, TPK1, TPP1, TRA2B, TRAF7, TRAK1, TRAPPC12, TRAPPC4, TRAPPC6B, TREX1, TRIM8, TRIP13, TRIT1, TRPM3, TRPM6, TRPM7, TRRAP, TSC1, TSC2, TSEN15, TSEN2, TSEN34, TSEN54, TSFM, TTC19, TUBA1A, TUBA8, TUBB, TUBB2A, TUBB2B, TUBB3, TUBB4A, TUBG1, TUBGCP2, TXNRD1, U2AF2, UBA5, UBAP2L, UBE2A, UBE3A, UBR5, UBR7, UBTF, UFC1, UFM1, UFSP2, UGDH, UGGT1, UGP2, UNC13A, UNC80, USP18, USP25, USP7, VAMP2, VARS1, VLDLR, VPS11, VPS13A, VPS50, WARS2, WASF1, WDR26, WDR37, WDR45, WDR45B, WDR47, WDR62, WDR73, WNK3, WWOX, XK, YIF1B, YIPF5, YWHAG, YY1, ZBTB18, ZBTB47, ZDHHC9, ZEB2, ZFYVE26, ZMIZ1, ZMYM2, ZNF142, ZNF335, ZNFX1, ZNHIT3, ZSWIM6

GC_54 Idiopatic Epilepsy

Idiopathic or genetic epilepsies comprise a group of epilepsy syndromes in which seizures occur without an identified acquired structural cause and in which genetic factors are considered to play an important role. These disorders may include generalized as well as selected focal or non-lesional epilepsy syndromes and often occur in individuals without major developmental abnormalities.

This panel includes genes associated with genetic generalized and other non-lesional epilepsies, particularly disorders affecting neuronal ion channels, synaptic transmission, and other pathways involved in neuronal excitability.

This panel is recommended for patients with suspected genetic epilepsy in the absence of a clear acquired structural cause, particularly when brain imaging is normal and there is no significant developmental delay or broader syndromic phenotype. Compared with the broader GC_23 – Epilepsy panel, this focused panel is preferred when epilepsy appears to be the primary or isolated clinical manifestation.

Last update: 16.01.2026

ALDH7A1, AMACR, ATP6V0C, CACNA1A, CACNA1H, CACNB4, CASR, CHRNA2, CHRNA4, CHRNB2, CLCN2, DEPDC5, EFHC1, GABRA1, GABRB3, GABRG2, GNAO1, GRIN2A, HCN1, HCN2, KCNA1, KCNC1, KCNMA1, KCNQ2, KCNQ3, KCNT1, LGI1, MTOR, NPRL2, NPRL3, PCDH19, POLG, PRRT2, RELN, RORB, SCN1A, SCN1B, SCN2A, SCN3A, SCN8A, SCN9A, SLC2A1, SLC32A1, SLC6A1, STX1B, TBC1D24, USP25

ClinVar P/LP variants (IDs) not covered: GABRG2:[3757681] | SCN1A:[4538527]

GC_61 Brain Malformation

Last update: 07.01.2026

ACTB, ACTG1, ADGRG1, ADNP, AHDC1, AHI1, AKT1, AKT3, AMPD2, APC2, ARF1, ARFGEF2, ARID1A, ARID1B, ARX, ASNS, ASPM, ATP1A2, ATP1A3, ATP6V0A2, B3GALNT2, B4GAT1, BMP4, C19ORF12, CASK, CASP2, CCM2, CCND2, CDH2, CDK13, CDK5, CDK5RAP2, CDON, CENPE, CEP152, CEP85L, CHMP1A, CHN1, CIT, CNOT1, CNOT3, COASY, COL18A1, COL3A1, COL4A1, COL4A2, CP, CRADD, CRPPA, CSNK2A1, CTNNA2, CUL4B, DAG1, DCC, DCHS1, DCX, DEPDC5, DHCR7, DIAPH1, DISP1, DLL1, DMXL2, DOCK6, DPF2, DPYSL5, DYNC1H1, EIF2AK2, EMC1, EML1, EMX2, ERMARD, EXOSC3, FA2H, FAT4, FGF8, FGFR1, FIG4, FKRP, FKTN, FLNA, FOXA2, FTL, GAS1, GLI2, GMPPB, GPSM2, GRIN1, GRIN2B, H3-3A, HECTD4, HIVEP2, HS2ST1, IER3IP1, IQSEC2, KATNB1, KCNMA1, KIF11, KIF21A, KIF26A, KIF2A, KIF5C, KIF7, KIFBP, KMT2D, KMT2E, KRIT1, L1CAM, LAMA1, LAMA2, LAMB1, LAMC3, LARGE1, LRP2, MACF1, MAP1B, MAPK8IP3, MAX, MED12, MED17, MFSD2A, MN1, MRE11, MTOR, NDE1, NEDD4L, NFIA, NPRL2, NPRL3, NSRP1, OCLN, OPHN1, OSGEP, PAFAH1B1, PANK2, PDCD10, PEX1, PEX10, PEX11B, PEX12, PEX13, PEX14, PEX16, PEX19, PEX2, PEX26, PEX3, PEX5, PEX6, PHGDH, PI4KA, PIDD1, PIK3CA, PIK3R2, PLA2G6, PLCH1, PNKP, POMGNT1, POMGNT2, POMK, POMT1, POMT2, PPP1R12A, PROK2, PROKR2, PTCH1, PTEN, QARS1, RAB11B, RAB18, RAB3GAP1, RAB3GAP2, RAC3, RAD21, RARS2, RASA1, RBM10, RELN, RERE, ROBO3, RTTN, RXYLT1, SCN3A, SEPSECS, SHH, SIN3A, SIX3, SLC25A19, SLC35A2, SMARCA4, SMARCB1, SMARCC1, SMARCE1, SMC1A, SMO, SNAP29, SON, SOX11, SOX2, SRD5A3, STAG2, STAMBP, STIL, SUFU, TBC1D20, TBC1D32, TGIF1, TMTC3, TMX2, TOE1, TP73, TRRAP, TSC1, TSEN2, TSEN34, TSEN54, TUBA1A, TUBA8, TUBB, TUBB2A, TUBB2B, TUBB3, TUBB4A, TUBG1, TUBGCP2, TUBGCP6, UBE3B, USP7, USP9X, VLDLR, VPS13A, VPS50, VRK1, WDR45, WDR62, WNK3, YWHAE, ZBTB18, ZBTB20, ZIC2, ZMIZ1

ClinVar P/LP variants (IDs) not covered: ARID1B:[3378371] | PANK2:[3897668] | PEX14:[3663959] | PTEN:[2587202]

GC_64 Cerebral Small Vessel

Last update: 07.01.2026

ABCC6, APP, ARHGEF15, ATP1A2, CACNA1A, CBS, CCM2, COL3A1, COL4A1, COL4A2, COLGALT1, CST3, CTSA, ESAM, FOXC1, GLA, HTRA1, KRIT1, NIT1, NOTCH3, PDCD10, TREX1

ClinVar P/LP variants (IDs) not covered: GLA: [1678527]

GC_86 Microcephaly

Last update: 04.01.2026

AARS1, ACBD6, ADARB1, AFG2B, AGMO, AKT3, AMPD2, ANKLE2, AP4B1, AP4E1, AP4M1, AP4S1, ARCN1, ARF3, ARPC4, ASPM, ASXL1, ASXL3, ATP1A2, ATP6V0A1, ATP6V0C, ATP9A, ATR, ATRX, BLM, BPTF, BRCA2, BRD4, BRIP1, BUB1, BUB1B, CAMK2B, CAMSAP1, CASK, CCDC47, CCDC88A, CCND2, CDK5RAP2, CDT1, CENPF, CENPJ, CEP135, CEP152, CEP295, CEP55, CEP57, CEP63, CHAMP1, CHKA, CHMP1A, CIT, CKAP2L, COASY, COG3, COPB1, CPAP, CPSF3, CREBBP, CRIPT, CRNKL1, CSNK2A1, CTCF, CTNNB1, CTU2, DDX11, DHCR7, DIAPH1, DNA2, DNMT3A,

DOHH, DONSON, DPM1, DROSHA, DYNC1H1, DYNC1I2, DYRK1A, EEF1D, EFTUD2, EIF2S3, EIF5A, ERCC4, ERCC5, ERCC6, ERCC8, EXOC7, EXOSC3, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FBRSL1, FILIP1, FLVCR1, FOXG1, FRA10AC1, GFM1, GINS3, GMNN, GPKOW, GPT2, GRM7, GTF2E2, GTF3C3, H4C3, HDAC8, HHAT, HMGB1, HPDL, IARS1, IER3IP1, IGF1, IGF1R, INPP4A, INTS11, KANSL1, KATNB1, KBTBD2, KIF11, KIF14, KIFBP,

KMT2B, KNL1, LAGE3, LARP7, LHX2, LIG4, LMNB1, LMNB2, LRRC8C, MBD5, MCM7, MCPH1, MECP2, MED11, MED17, METTL5, MFSD2A, MINPP1, MIPEP, MIR17HG, MORC2, MPLKIP, MRE11, MRPL49, MSMO1, MYCN, MYO18B, NAA20, NAPB, NARS1, NBN, NCAPD2, NCAPD3, NCAPH, NDE1, NHEJ1, NIPBL, NSD2, NSRP1, NUP107, NUP188, NUP214, OPHN1, ORC1, ORC4, ORC6, OSGEP, PAFAH1B1, PALB2, PCDH12, PCDHGC4, PCLO, PCNT, PDCD6IP, PDHA1, PHGDH, PLK4, PNKP, PNPLA8, POC1A, POGZ, POMT1, PPFIBP1, PPIL1, PPP1R15B, PQBP1, PRIM1, PRUNE1,

PSMC3, PTPMT1, PTPN23, PUF60, PUS7, QARS1, RAD21, RAD50, RAD51, RAD51C, RARS2, RBBP8, RMI1, RNU4-2, RNU4ATAC, RPL10, RRP7A, RTTN, SARS1, SASS6, SEPSECS, SLC1A4, SLC25A19, SLC38A3, SLC4A10, SLC9A6, SLF2, SLX4, SMARCA2, SMARCA5, SMARCE1, SMC1A, SMC3, SMC5, SMG8, SOX11, SPATA5L1, SPOUT1, STAG2, STAMBP, STIL, SVBP, TAF13, TBC1D20, TBC1D23, THOC6, TMEM167A, TMTC3, TMX2, TNPO2, TOE1, TOP3A, TP53RK, TRA2B, TRAIP, TRAPPC10, TRAPPC12, TRAPPC14, TRAPPC4, TRAPPC6B, TRAPPC9, TRIO, TRIP13, TRMT10A, TSEN15, TSEN2, TSEN54, TTC5, TTI1, TUBB, TUBB2B, TUBG1, TUBGCP2, TUBGCP4, TUBGCP6, UBA5, UBE3A, UBE3B, UFC1, UFM1, UGGT1, UGP2, UNC80, VARS1, VPS50, VRK1, WARS1, WDR11, WDR37, WDR4, WDR47, WDR62, WDR73, WLS, XRCC4, YIF1B, YIPF5, ZEB2, ZNF148, ZNF335, ZNF526, ZNF668

ClinVar P/LP variants (IDs) not covered: ASXL3:4291910 | BRCA2:3780838 | CTNNB1:4293194

| RAD51C:3228945; 2625143 | WDR4:3377309 | ZEB2:3770192