{{Rsnum
|rsid=118192249
|Chromosome=8
|position=132175461
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=KCNQ3
|Gene_s=KCNQ3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Orientation=minus
}}{{ClinVar
|ALT=G
|CHROM=8
|CLNACC=RCV000020601.1
|CLNALLE=1
|CLNDBN=Benign familial neonatal seizures 2
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK32534:C1852581:121201:1949
|CLNHGVS=NC_000008.10:g.133187708A>G
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK32534
|Disease=Benign familial neonatal seizures 2
|FwdALT=C
|FwdREF=T
|GENEINFO=KCNQ3:3786
|GENE_ID=3786
|GENE_NAME=KCNQ3
|REF=A
|RSPOS=133187708
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;S3D;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050360000000000002110100
|WGT=0
|dbSNPBuildID=132
|rsid=118192249
}}