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rs7765175

From SNPedia

Orientationplus
Stabilizedplus
Make rs7765175(C;C)
Make rs7765175(C;T)
Make rs7765175(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position113344125
is asnp
is mentioned by
dbSNPrs7765175
ebirs7765175
HLIrs7765175
Exacrs7765175
Varsomers7765175
Maprs7765175
PheGenIrs7765175
hapmaprs7765175
1000 genomesrs7765175
hgdprs7765175
ensemblrs7765175
gopubmedrs7765175
geneviewrs7765175
scholarrs7765175
googlers7765175
pharmgkbrs7765175
gwascentralrs7765175
openSNPrs7765175
23andMers7765175
23andMe allrs7765175
SNP Nexus

SNPshotrs7765175
SNPdbers7765175
MSV3drs7765175
GWAS Ctlgrs7765175
GMAF0.2736
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 5E-6
Odds Ratio .21 [0.11-0.31] unit decrease