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rs2201728

From SNPedia

Orientationplus
Stabilizedplus
Make rs2201728(A;A)
Make rs2201728(A;G)
Make rs2201728(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position99242716
GeneLOC100507053
is asnp
is mentioned by
dbSNPrs2201728
dbSNP (classic)rs2201728
ClinGenrs2201728
ebirs2201728
HLIrs2201728
Exacrs2201728
Gnomadrs2201728
Varsomers2201728
LitVarrs2201728
Maprs2201728
PheGenIrs2201728
Biobankrs2201728
1000 genomesrs2201728
hgdprs2201728
ensemblrs2201728
geneviewrs2201728
scholarrs2201728
googlers2201728
pharmgkbrs2201728
gwascentralrs2201728
openSNPrs2201728
23andMers2201728
SNPshotrs2201728
SNPdbers2201728
MSV3drs2201728
GWAS Ctlgrs2201728
GMAF0.3347
Max Magnitude0
? (A;A) (A;G) (G;G) 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 G
P-val 5E-6
Odds Ratio 3.13 [1.92-5]