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rs11886999

From SNPedia

Orientationplus
Stabilizedplus
Make rs11886999(C;C)
Make rs11886999(C;T)
Make rs11886999(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position96176055
is asnp
is mentioned by
dbSNPrs11886999
ebirs11886999
HLIrs11886999
Exacrs11886999
Varsomers11886999
Maprs11886999
PheGenIrs11886999
hapmaprs11886999
1000 genomesrs11886999
hgdprs11886999
ensemblrs11886999
gopubmedrs11886999
geneviewrs11886999
scholarrs11886999
googlers11886999
pharmgkbrs11886999
gwascentralrs11886999
openSNPrs11886999
23andMers11886999
23andMe allrs11886999
SNP Nexus

SNPshotrs11886999
SNPdbers11886999
MSV3drs11886999
GWAS Ctlgrs11886999
GMAF0.2438
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 8E-6
Odds Ratio .04 [0.02-0.06] ug/L increase