{{Rsnum
|rsid=118192197
|Chromosome=20
|Orientation=minus
|geno1=(A;A)
|geno2=(A;CTGCGCTCCG)
|geno3=(CTGCGCTCCG;CTGCGCTCCG)
|Gene=KCNQ2
|position=63444756
|Gene_s=KCNQ2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=CT
|CHROM=20
|CLNACC=RCV000020998.1
|CLNALLE=1
|CLNDBN=Benign familial neonatal seizures 1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK32534:C1852587:121200:1949
|CLNHGVS=NC_000020.10:g.62076109_62076118delCGGAGCGCAGinsT
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK32534
|Disease=Benign familial neonatal seizures 1
|FwdALT=A
|FwdREF=CTGCGCTCCG
|GENEINFO=KCNQ2:3785
|GENE_ID=3785
|GENE_NAME=KCNQ2
|REF=CCGGAGCGCAG
|RSPOS=62076108
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050160000000000002110200
|WGT=0
|dbSNPBuildID=132
|rsid=118192197
}}