{{Rsnum
|rsid=118192250
|Chromosome=8
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=KCNQ3
|position=132175457
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KCNQ3
}}{{omim
|id=602232
|rsnum=118192250
|variant=0001
}}{{ClinVar
|rsid=118192250
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=133187704
|CHROM=8
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050360000000000002110100
|GENEINFO=KCNQ3:3786
|GENE_NAME=KCNQ3
|GENE_ID=3786
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000008.10:g.133187704C>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK32534; 602232.0001
|CLNSIG=5
|CLNCUI=C1852581
|CLNDBN=Benign familial neonatal seizures 2
|Disease=Benign familial neonatal seizures 2
|CLNACC=RCV000007816.1
|Tags=RV;PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK32534:C1852581:121201:1949
}}