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rs9506514

From SNPedia

Orientationplus
Stabilizedplus
Make rs9506514(A;A)
Make rs9506514(A;C)
Make rs9506514(C;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position20557072
is asnp
is mentioned by
dbSNPrs9506514
ebirs9506514
HLIrs9506514
Exacrs9506514
Varsomers9506514
Maprs9506514
PheGenIrs9506514
hapmaprs9506514
1000 genomesrs9506514
hgdprs9506514
ensemblrs9506514
gopubmedrs9506514
geneviewrs9506514
scholarrs9506514
googlers9506514
pharmgkbrs9506514
gwascentralrs9506514
openSNPrs9506514
23andMers9506514
23andMe allrs9506514
SNP Nexus

SNPshotrs9506514
SNPdbers9506514
MSV3drs9506514
GWAS Ctlgrs9506514
GMAF0.4927
Max Magnitude
? (A;A) (A;C) (C;C) 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 5E-6
Odds Ratio .17 [0.092-0.248] unit decrease