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rs796052677

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052677(A;G)
Make rs796052677(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position132175589
GeneKCNQ3
is asnp
is mentioned by
dbSNPrs796052677
ebirs796052677
HLIrs796052677
Exacrs796052677
Varsomers796052677
Maprs796052677
PheGenIrs796052677
hapmaprs796052677
1000 genomesrs796052677
hgdprs796052677
ensemblrs796052677
gopubmedrs796052677
geneviewrs796052677
scholarrs796052677
googlers796052677
pharmgkbrs796052677
gwascentralrs796052677
openSNPrs796052677
23andMers796052677
23andMe allrs796052677
SNP Nexus

SNPshotrs796052677
SNPdbers796052677
MSV3drs796052677
GWAS Ctlgrs796052677
Max Magnitude0
ClinVar
Risk rs796052677(G;G)
Alt rs796052677(G;G)
Reference rs796052677(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ3
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.133187836T>C
CLNSRC
CLNACC RCV000187969.2,