{{Rsnum
|rsid=117067974
|Gene=KCNQ2
|Chromosome=20
|position=63414174
|Orientation=plus
|GMAF=0.0101
|Gene_s=KCNQ2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
}}{{ClinVar
|rsid=117067974
|Reversed=0
|FwdREF=C
|FwdALT=A,G
|REF=C
|ALT=A,G
|RSPOS=62045527
|CHROM=20
|GMAF=0.0101
|dbSNPBuildID=132
|SSR=0
|SAO=0
|VP=0x050160000000170416110100
|GENEINFO=KCNQ2:3785
|GENE_NAME=KCNQ2
|GENE_ID=3785
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000020.10:g.62045527C>G
|CLNSRC=GeneReviews
|CLNSRCID=NBK32534
|CLNSIG=5
|CLNCUI=C1852587
|CLNDBN=Benign familial neonatal seizures 1
|Disease=Benign familial neonatal seizures 1
|CLNACC=RCV000020972.1
|Tags=PM;SLO;VLD;G5A;G5;HD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9899; 0.0101
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK32534:C1852587:121200:1949
|COMMON=1
}}
{{omim
|id=121200
|rsnum=117067974
}}