Have questions? Visit https://www.reddit.com/r/SNPedia

rs12210810

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs12210810(C;C)
Make rs12210810(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position118332041
is asnp
is mentioned by
dbSNPrs12210810
ebirs12210810
HLIrs12210810
Exacrs12210810
Varsomers12210810
Maprs12210810
PheGenIrs12210810
hapmaprs12210810
1000 genomesrs12210810
hgdprs12210810
ensemblrs12210810
gopubmedrs12210810
geneviewrs12210810
scholarrs12210810
googlers12210810
pharmgkbrs12210810
gwascentralrs12210810
openSNPrs12210810
23andMers12210810
23andMe allrs12210810
SNP Nexus

SNPshotrs12210810
SNPdbers12210810
MSV3drs12210810
GWAS Ctlgrs12210810
GMAF0.02204
Max Magnitude0
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 19305409OA-icon.png]
Trait QT interval
Title Common variants at ten loci modulate the QT interval duration in the QTSCD Study
Risk Allele C
P-val 2E-17
Odds Ratio 3.13 [2.29-3.97] ms decrease



GET Evidence
rs12210810
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.015625
summary