{{Rsnum
|rsid = 28939683
|Gene = KCNQ2
|Orientation=minus
|ReferenceAllele=A
|MissenseAllele=G
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Chromosome=20
|position=63439674
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KCNQ2
}}{{omim
|desc=EPILEPSY, BENIGN NEONATAL, 1
|id=602235
|rsnum=28939683
|variant=0001
}}

{{ClinVar
|rsid=28939683
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=62071027
|CHROM=20
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050360000000000002110100
|GENEINFO=KCNQ2:3785
|GENE_NAME=KCNQ2
|GENE_ID=3785
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000020.10:g.62071027T>C
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK32534; 602235.0001
|CLNSIG=5
|CLNCUI=C1852587; C1852587
|CLNDBN=Benign familial neonatal seizures 1
|Disease=Benign familial neonatal seizures 1
|CLNACC=RCV000007806.1
|Tags=RV;PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK32534:C1852587:121200:1949
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}