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rs10091374

From SNPedia

Orientationplus
Stabilizedplus
Make rs10091374(A;A)
Make rs10091374(A;T)
Make rs10091374(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position70474669
GeneLOC101926892
is asnp
is mentioned by
dbSNPrs10091374
dbSNP (classic)rs10091374
ClinGenrs10091374
ebirs10091374
HLIrs10091374
Exacrs10091374
Gnomadrs10091374
Varsomers10091374
LitVarrs10091374
Maprs10091374
PheGenIrs10091374
Biobankrs10091374
1000 genomesrs10091374
hgdprs10091374
ensemblrs10091374
geneviewrs10091374
scholarrs10091374
googlers10091374
pharmgkbrs10091374
gwascentralrs10091374
openSNPrs10091374
23andMers10091374
SNPshotrs10091374
SNPdbers10091374
MSV3drs10091374
GWAS Ctlgrs10091374
GMAF0.4871
Max Magnitude0
? (A;A) (A;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 A
P-val 9E-9
Odds Ratio .04 [0.027-0.059] ug/L decrease