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rs6473383

From SNPedia

Orientationplus
Stabilizedplus
Make rs6473383(A;A)
Make rs6473383(A;G)
Make rs6473383(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position82756885
is asnp
is mentioned by
dbSNPrs6473383
ebirs6473383
HLIrs6473383
Exacrs6473383
Varsomers6473383
Maprs6473383
PheGenIrs6473383
hapmaprs6473383
1000 genomesrs6473383
hgdprs6473383
ensemblrs6473383
gopubmedrs6473383
geneviewrs6473383
scholarrs6473383
googlers6473383
pharmgkbrs6473383
gwascentralrs6473383
openSNPrs6473383
23andMers6473383
23andMe allrs6473383
SNP Nexus

SNPshotrs6473383
SNPdbers6473383
MSV3drs6473383
GWAS Ctlgrs6473383
GMAF0.1501
Max Magnitude
? (A;A) (A;G) (G;G) 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 0.000003
Odds Ratio 1.19 [0.99-1.44]