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rs899967

From SNPedia

Orientationplus
Stabilizedplus
Make rs899967(C;C)
Make rs899967(C;G)
Make rs899967(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position63192088
GeneBCL2
is asnp
is mentioned by
dbSNPrs899967
ebirs899967
HLIrs899967
Exacrs899967
Varsomers899967
Maprs899967
PheGenIrs899967
hapmaprs899967
1000 genomesrs899967
hgdprs899967
ensemblrs899967
gopubmedrs899967
geneviewrs899967
scholarrs899967
googlers899967
pharmgkbrs899967
gwascentralrs899967
openSNPrs899967
23andMers899967
23andMe allrs899967
SNP Nexus

SNPshotrs899967
SNPdbers899967
MSV3drs899967
GWAS Ctlgrs899967
GMAF0.399
Max Magnitude
? (C;C) (C;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 C
P-val 7E-6
Odds Ratio .04 [0.02-0.05] ug/L decrease