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rs10812610

From SNPedia

Orientationplus
Stabilizedplus
Make rs10812610(A;A)
Make rs10812610(A;C)
Make rs10812610(C;C)
ReferenceGRCh38 38.1/141
Chromosome9
Position27533986
is asnp
is mentioned by
dbSNPrs10812610
ebirs10812610
HLIrs10812610
Exacrs10812610
Varsomers10812610
Maprs10812610
PheGenIrs10812610
hapmaprs10812610
1000 genomesrs10812610
hgdprs10812610
ensemblrs10812610
gopubmedrs10812610
geneviewrs10812610
scholarrs10812610
googlers10812610
pharmgkbrs10812610
gwascentralrs10812610
openSNPrs10812610
23andMers10812610
23andMe allrs10812610
SNP Nexus

SNPshotrs10812610
SNPdbers10812610
MSV3drs10812610
GWAS Ctlgrs10812610
GMAF0.4807
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 20445134OA-icon.png]
Trait Heart failure
Title The Association of Genome-Wide Variation with the Risk of Incident Heart Failure in Adults of European and African Ancestry: A Prospective Meta-Analysis from the CHARGE Consortium
Risk Allele
P-val 0.000005
Odds Ratio 1.14 [0.99-1.31]