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rs12151790

From SNPedia

Orientationplus
Stabilizedplus
Make rs12151790(A;A)
Make rs12151790(A;G)
Make rs12151790(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position234302083
is asnp
is mentioned by
dbSNPrs12151790
ebirs12151790
HLIrs12151790
Exacrs12151790
Varsomers12151790
Maprs12151790
PheGenIrs12151790
hapmaprs12151790
1000 genomesrs12151790
hgdprs12151790
ensemblrs12151790
gopubmedrs12151790
geneviewrs12151790
scholarrs12151790
googlers12151790
pharmgkbrs12151790
gwascentralrs12151790
openSNPrs12151790
23andMers12151790
23andMe allrs12151790
SNP Nexus

SNPshotrs12151790
SNPdbers12151790
MSV3drs12151790
GWAS Ctlgrs12151790
GMAF0.1313
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20548944OA-icon.png]
Trait Osteoporosis
Title An Integration of Genome-Wide Association Study and

Gene Expression Profiling to Prioritize the Discovery of Novel Susceptibility Loci for Osteoporosis-Related Traits

Risk Allele A
P-val 5E-7
Odds Ratio 0.40 [NR] g/cm2 increase