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rs796052637

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052637(A;G)
Make rs796052637(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63439677
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs796052637
ebirs796052637
HLIrs796052637
Exacrs796052637
Varsomers796052637
Maprs796052637
PheGenIrs796052637
hapmaprs796052637
1000 genomesrs796052637
hgdprs796052637
ensemblrs796052637
gopubmedrs796052637
geneviewrs796052637
scholarrs796052637
googlers796052637
pharmgkbrs796052637
gwascentralrs796052637
openSNPrs796052637
23andMers796052637
23andMe allrs796052637
SNP Nexus

SNPshotrs796052637
SNPdbers796052637
MSV3drs796052637
GWAS Ctlgrs796052637
Max Magnitude0
ClinVar
Risk rs796052637(G;G)
Alt rs796052637(G;G)
Reference rs796052637(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62071030T>C
CLNSRC
CLNACC RCV000187882.2,