Have questions? Visit https://www.reddit.com/r/SNPedia

rs17666963

From SNPedia

Orientationplus
Stabilizedplus
Make rs17666963(C;C)
Make rs17666963(C;T)
Make rs17666963(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position123447985
is asnp
is mentioned by
dbSNPrs17666963
ebirs17666963
HLIrs17666963
Exacrs17666963
Varsomers17666963
Maprs17666963
PheGenIrs17666963
hapmaprs17666963
1000 genomesrs17666963
hgdprs17666963
ensemblrs17666963
gopubmedrs17666963
geneviewrs17666963
scholarrs17666963
googlers17666963
pharmgkbrs17666963
gwascentralrs17666963
openSNPrs17666963
23andMers17666963
23andMe allrs17666963
SNP Nexus

SNPshotrs17666963
SNPdbers17666963
MSV3drs17666963
GWAS Ctlgrs17666963
GMAF0.09137
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 9E-6
Odds Ratio 2.28 [1.58-3.28]