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rs13083990

From SNPedia

Orientationplus
Stabilizedplus
Make rs13083990(C;C)
Make rs13083990(C;T)
Make rs13083990(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position122295719
is asnp
is mentioned by
dbSNPrs13083990
ebirs13083990
HLIrs13083990
Exacrs13083990
Varsomers13083990
Maprs13083990
PheGenIrs13083990
hapmaprs13083990
1000 genomesrs13083990
hgdprs13083990
ensemblrs13083990
gopubmedrs13083990
geneviewrs13083990
scholarrs13083990
googlers13083990
pharmgkbrs13083990
gwascentralrs13083990
openSNPrs13083990
23andMers13083990
23andMe allrs13083990
SNP Nexus

SNPshotrs13083990
SNPdbers13083990
MSV3drs13083990
GWAS Ctlgrs13083990
GMAF0.3453
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 2.66 [1.76-4.02]


[PMID 23125333OA-icon.png] Common genetic variation of the calcium-sensing receptor and lethal prostate cancer risk.