{{Rsnum
|rsid=118192196
|Chromosome=20
|Orientation=minus
|geno1=(-;-)
|geno2=(-;AGG)
|geno3=(AGG;AGG)
|Gene=KCNQ2
|position=63445364
|Gene_s=KCNQ2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=20
|CLNACC=RCV000020997.1
|CLNALLE=1
|CLNDBN=Benign familial neonatal seizures 1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK32534:C1852587:121200:1949
|CLNHGVS=NC_000020.10:g.62076717_62076719delCCT
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK32534
|Disease=Benign familial neonatal seizures 1
|FwdREF=GGA
|GENEINFO=KCNQ2:3785
|GENE_ID=3785
|GENE_NAME=KCNQ2
|REF=TCCT
|RSPOS=62076716
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050160000000000002110200
|WGT=0
|dbSNPBuildID=132
|rsid=118192196
}}