{{Rsnum
|rsid=397507449
|Chromosome=20
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=KCNQ2
|position=63433808
|Gene_s=KCNQ2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=20
|CLNACC=RCV000020966.2
|CLNALLE=1
|CLNDBN=Benign familial neonatal seizures 1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK32534:C1852587:121200:1949
|CLNHGVS=NC_000020.10:g.62065161C>T
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK32534
|Disease=Benign familial neonatal seizures 1
|FwdALT=A
|FwdREF=G
|REF=C
|RSPOS=62065161
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=397507449
|GENEINFO=KCNQ2:3785
|GENE_ID=3785
|GENE_NAME=KCNQ2
}}