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rs17772222

From SNPedia

Orientationplus
Stabilizedplus
Make rs17772222(A;A)
Make rs17772222(A;G)
Make rs17772222(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position88360138
is asnp
is mentioned by
dbSNPrs17772222
ebirs17772222
HLIrs17772222
Exacrs17772222
Varsomers17772222
Maprs17772222
PheGenIrs17772222
hapmaprs17772222
1000 genomesrs17772222
hgdprs17772222
ensemblrs17772222
gopubmedrs17772222
geneviewrs17772222
scholarrs17772222
googlers17772222
pharmgkbrs17772222
gwascentralrs17772222
openSNPrs17772222
23andMers17772222
23andMe allrs17772222
SNP Nexus

SNPshotrs17772222
SNPdbers17772222
MSV3drs17772222
GWAS Ctlgrs17772222
GMAF0.2484
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 3E-6
Odds Ratio .21 [0.13-0.29] unit decrease