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rs9907236

From SNPedia

Orientationplus
Stabilizedplus
Make rs9907236(A;A)
Make rs9907236(A;G)
Make rs9907236(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position71493932
is asnp
is mentioned by
dbSNPrs9907236
ebirs9907236
HLIrs9907236
Exacrs9907236
Varsomers9907236
Maprs9907236
PheGenIrs9907236
hapmaprs9907236
1000 genomesrs9907236
hgdprs9907236
ensemblrs9907236
gopubmedrs9907236
geneviewrs9907236
scholarrs9907236
googlers9907236
pharmgkbrs9907236
gwascentralrs9907236
openSNPrs9907236
23andMers9907236
23andMe allrs9907236
SNP Nexus

SNPshotrs9907236
SNPdbers9907236
MSV3drs9907236
GWAS Ctlgrs9907236
GMAF0.06749
Max Magnitude
? (A;A) (A;G) (G;G) 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 A
P-val 2E-6
Odds Ratio .51 [0.29-0.73] unit increase