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rs12808199

From SNPedia

Orientationplus
Stabilizedplus
Make rs12808199(A;A)
Make rs12808199(A;G)
Make rs12808199(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position39306409
is asnp
is mentioned by
dbSNPrs12808199
ebirs12808199
HLIrs12808199
Exacrs12808199
Varsomers12808199
Maprs12808199
PheGenIrs12808199
hapmaprs12808199
1000 genomesrs12808199
hgdprs12808199
ensemblrs12808199
gopubmedrs12808199
geneviewrs12808199
scholarrs12808199
googlers12808199
pharmgkbrs12808199
gwascentralrs12808199
openSNPrs12808199
23andMers12808199
23andMe allrs12808199
SNP Nexus

SNPshotrs12808199
SNPdbers12808199
MSV3drs12808199
GWAS Ctlgrs12808199
GMAF0.4582
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 G
P-val 9E-7
Odds Ratio 0.21 [NR] g/cm2 decrease