{{Rsnum
|rsid=74315391
|Gene=KCNQ2
|Chromosome=20
|position=63444730
|Orientation=minus
|GMAF=0.0
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=KCNQ2
}}{{omim
|id=602235
|rsnum=74315391
|variant=0006
}}{{ClinVar
|rsid=74315391
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=62076083
|CHROM=20
|GMAF=0
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050360000000040016110100
|GENEINFO=KCNQ2:3785
|GENE_NAME=KCNQ2
|GENE_ID=3785
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000020.10:g.62076083G>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK32534; 602235.0006
|CLNSIG=5
|CLNCUI=C1852587
|CLNDBN=Seizures, benign familial neonatal, 1, and/or myokymia; Benign familial neonatal seizures 1
|Disease=Seizures; Benign familial neonatal seizures 1
|CLNACC=RCV000007811.1; RCV000021001.1
|Tags=RV;PM;S3D;SLO;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=1; 0
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK32534:C1852587:121200:1949
|COMMON=0
}}