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rs9321637

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs9321637(C;C)
Make rs9321637(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position137945548
is asnp
is mentioned by
dbSNPrs9321637
ebirs9321637
HLIrs9321637
Exacrs9321637
Varsomers9321637
Maprs9321637
PheGenIrs9321637
hapmaprs9321637
1000 genomesrs9321637
hgdprs9321637
ensemblrs9321637
gopubmedrs9321637
geneviewrs9321637
scholarrs9321637
googlers9321637
pharmgkbrs9321637
gwascentralrs9321637
openSNPrs9321637
23andMers9321637
23andMe allrs9321637
SNP Nexus

SNPshotrs9321637
SNPdbers9321637
MSV3drs9321637
GWAS Ctlgrs9321637
GMAF0.1391
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 22355377OA-icon.png] Caucasian and asian specific rheumatoid arthritis risk Loci reveal limited replication and apparent allelic heterogeneity in north indians
GWAS snp
PMID [PMID 23247143OA-icon.png]
Trait Cardiac Troponin-T levels
Title Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European americans and blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies.
Risk Allele C
P-val 8E-6
Odds Ratio 2.17 [1.56-3.13]