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rs11760067

From SNPedia

Orientationplus
Stabilizedplus
Make rs11760067(C;C)
Make rs11760067(C;T)
Make rs11760067(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position134773134
is asnp
is mentioned by
dbSNPrs11760067
ebirs11760067
HLIrs11760067
Exacrs11760067
Varsomers11760067
Maprs11760067
PheGenIrs11760067
hapmaprs11760067
1000 genomesrs11760067
hgdprs11760067
ensemblrs11760067
gopubmedrs11760067
geneviewrs11760067
scholarrs11760067
googlers11760067
pharmgkbrs11760067
gwascentralrs11760067
openSNPrs11760067
23andMers11760067
23andMe allrs11760067
SNP Nexus

SNPshotrs11760067
SNPdbers11760067
MSV3drs11760067
GWAS Ctlgrs11760067
GMAF0.06198
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23870195OA-icon.png]
Trait Coronary artery calcification
Title Genetics of coronary artery calcification among African Americans, a meta-analysis.
Risk Allele T
P-val 7E-6
Odds Ratio .80 [0.45-1.15] unit increase