{{Rsnum
|rsid=74315392
|Chromosome=20
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=KCNQ2
|position=63442482
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KCNQ2
}}{{omim
|id=602235
|rsnum=74315392
|variant=0008
}}{{ClinVar
|rsid=74315392
|Reversed=1
|FwdREF=C
|FwdALT=A,G
|REF=G
|ALT=C,T
|RSPOS=62073835
|CHROM=20
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050360000000000002110100
|GENEINFO=KCNQ2:3785
|GENE_NAME=KCNQ2
|GENE_ID=3785
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000020.10:g.62073835G>C; NC_000020.10:g.62073835G>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK32534; 602235.0008
|CLNSIG=5
|CLNCUI=C3150986; C1852587,C1852587
|CLNDBN=Early infantile epileptic encephalopathy 7; Benign familial neonatal seizures 1
|Disease=Early infantile epileptic encephalopathy 7; Benign familial neonatal seizures 1
|CLNACC=RCV000030664.1; RCV000030675.1; RCV000021009.1
|Tags=RV;PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=C3150986:613720:1934; NBK32534:C1852587:121200:1949
}}