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rs2341260

From SNPedia

Orientationplus
Stabilizedplus
Make rs2341260(C;C)
Make rs2341260(C;T)
Make rs2341260(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position73588377
is asnp
is mentioned by
dbSNPrs2341260
ebirs2341260
HLIrs2341260
Exacrs2341260
Varsomers2341260
Maprs2341260
PheGenIrs2341260
hapmaprs2341260
1000 genomesrs2341260
hgdprs2341260
ensemblrs2341260
gopubmedrs2341260
geneviewrs2341260
scholarrs2341260
googlers2341260
pharmgkbrs2341260
gwascentralrs2341260
openSNPrs2341260
23andMers2341260
23andMe allrs2341260
SNP Nexus

SNPshotrs2341260
SNPdbers2341260
MSV3drs2341260
GWAS Ctlgrs2341260
GMAF0.1474
Max Magnitude
? (C;C) (C;T) (T;T) 28
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 T
P-val 4E-6
Odds Ratio .05 [0.03-0.07] ug/L decrease