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rs2210327

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs2210327(A;A)
Make rs2210327(A;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position18109237
is asnp
is mentioned by
dbSNPrs2210327
ebirs2210327
HLIrs2210327
Exacrs2210327
Varsomers2210327
Maprs2210327
PheGenIrs2210327
hapmaprs2210327
1000 genomesrs2210327
hgdprs2210327
ensemblrs2210327
gopubmedrs2210327
geneviewrs2210327
scholarrs2210327
googlers2210327
pharmgkbrs2210327
gwascentralrs2210327
openSNPrs2210327
23andMers2210327
23andMe allrs2210327
SNP Nexus

SNPshotrs2210327
SNPdbers2210327
MSV3drs2210327
GWAS Ctlgrs2210327
GMAF0.1019
Max Magnitude0
? (A;A) (A;T) (T;T) 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 7E-7
Odds Ratio 3.14 [0.99-10.00]