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rs2957137

From SNPedia

Orientationplus
Stabilizedplus
Make rs2957137(A;A)
Make rs2957137(A;T)
Make rs2957137(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position62399655
is asnp
is mentioned by
dbSNPrs2957137
dbSNP (classic)rs2957137
ClinGenrs2957137
ebirs2957137
HLIrs2957137
Exacrs2957137
Gnomadrs2957137
Varsomers2957137
LitVarrs2957137
Maprs2957137
PheGenIrs2957137
Biobankrs2957137
1000 genomesrs2957137
hgdprs2957137
ensemblrs2957137
geneviewrs2957137
scholarrs2957137
googlers2957137
pharmgkbrs2957137
gwascentralrs2957137
openSNPrs2957137
23andMers2957137
SNPshotrs2957137
SNPdbers2957137
MSV3drs2957137
GWAS Ctlgrs2957137
GMAF0.4316
Max Magnitude0
? (A;A) (A;T) (T;T) 28


Rs2957137
PubMed [PMID 18445777]
Affy Probeset SNP_A-8507078
Affy Orientation reverse
On GW 5.0
Alleles A/B A/T
Ancestral T
Population Caucasian
Allele A
Case Freq.
Control Freq.
Odds Ratio Het
Odds Ratio Hom
Odds Ratio All 1.08
Disease Osteoporotic fractures (OP-F)


rs2957137 is in linkage disequilibrium with a polymorphism that increases susceptibility to Osteoporotic fractures 1.08 times for carriers of the A allele [PMID 18445777]