{{Rsnum
|rsid=118192231
|Chromosome=20
|Orientation=minus
|geno1=(-;-)
|geno2=(-;GCCCT)
|geno3=(GCCCT;GCCCT)
|Gene=KCNQ2
|position=63413528
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KCNQ2
}}{{omim
|id=602235
|rsnum=118192231
|variant=0003
}}{{ClinVar
|rsid=118192231
|Reversed=1
|FwdALT=GCCCT
|REF=T
|ALT=TAGGGC
|RSPOS=62044881
|CHROM=20
|dbSNPBuildID=132
|SSR=0
|SAO=0
|VP=0x050160000000000002110200
|GENEINFO=KCNQ2:3785
|GENE_NAME=KCNQ2
|GENE_ID=3785
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000020.10:g.62044881_62044882insAGGGC
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK32534; 602235.0003
|CLNSIG=5
|CLNCUI=C1852587; C1852587
|CLNDBN=Benign familial neonatal seizures 1
|Disease=Benign familial neonatal seizures 1
|CLNACC=RCV000007808.2
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK32534:C1852587:121200:1949
}}