{{Rsnum
|rsid=267607198
|Chromosome=20
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=KCNQ2
|position=63413551
|Gene_s=KCNQ2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=20
|CLNACC=RCV000007813.2; RCV000023180.2
|CLNALLE=1
|CLNDBN=Benign familial neonatal seizures 1; Early infantile epileptic encephalopathy 7
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; MedGen:OMIM:Orphanet
|CLNDSDBID=NBK32534:C1852587:121200:1949; C3150986:613720:1934
|CLNHGVS=NC_000020.10:g.62044904C>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=602235.0007
|Disease=Benign familial neonatal seizures 1; Early infantile epileptic encephalopathy 7
|FwdALT=T
|FwdREF=G
|GENEINFO=KCNQ2:3785
|GENE_ID=3785
|GENE_NAME=KCNQ2
|REF=C
|RSPOS=62044904
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267607198
}}