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rs796052613

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052613(C;G)
Make rs796052613(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63472242
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs796052613
ebirs796052613
HLIrs796052613
Exacrs796052613
Varsomers796052613
Maprs796052613
PheGenIrs796052613
hapmaprs796052613
1000 genomesrs796052613
hgdprs796052613
ensemblrs796052613
gopubmedrs796052613
geneviewrs796052613
scholarrs796052613
googlers796052613
pharmgkbrs796052613
gwascentralrs796052613
openSNPrs796052613
23andMers796052613
23andMe allrs796052613
SNP Nexus

SNPshotrs796052613
SNPdbers796052613
MSV3drs796052613
GWAS Ctlgrs796052613
Max Magnitude0
ClinVar
Risk rs796052613(G;G)
Alt rs796052613(G;G)
Reference rs796052613(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62103595G>C
CLNSRC
CLNACC RCV000187847.2,