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rs17088339

From SNPedia

Orientationplus
Stabilizedplus
Make rs17088339(A;A)
Make rs17088339(A;T)
Make rs17088339(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position73808898
is asnp
is mentioned by
dbSNPrs17088339
ebirs17088339
HLIrs17088339
Exacrs17088339
Varsomers17088339
Maprs17088339
PheGenIrs17088339
hapmaprs17088339
1000 genomesrs17088339
hgdprs17088339
ensemblrs17088339
gopubmedrs17088339
geneviewrs17088339
scholarrs17088339
googlers17088339
pharmgkbrs17088339
gwascentralrs17088339
openSNPrs17088339
23andMers17088339
23andMe allrs17088339
SNP Nexus

SNPshotrs17088339
SNPdbers17088339
MSV3drs17088339
GWAS Ctlgrs17088339
GMAF0.1065
Max Magnitude
? (A;A) (A;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 A
P-val 6E-6
Odds Ratio .68 [0.39-0.97] unit decrease