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rs2957128

From SNPedia

Orientationplus
Stabilizedplus
Make rs2957128(A;A)
Make rs2957128(A;G)
Make rs2957128(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position62393502
is asnp
is mentioned by
dbSNPrs2957128
ebirs2957128
HLIrs2957128
Exacrs2957128
Varsomers2957128
Maprs2957128
PheGenIrs2957128
hapmaprs2957128
1000 genomesrs2957128
hgdprs2957128
ensemblrs2957128
gopubmedrs2957128
geneviewrs2957128
scholarrs2957128
googlers2957128
pharmgkbrs2957128
gwascentralrs2957128
openSNPrs2957128
23andMers2957128
23andMe allrs2957128
SNP Nexus

SNPshotrs2957128
SNPdbers2957128
MSV3drs2957128
GWAS Ctlgrs2957128
GMAF0.4848
Max Magnitude
? (A;A) (A;G) (G;G) 28
related to Paget’s disease of bone 23andMe blog.
GWAS snp
PMID [PMID 20436471OA-icon.png]
Trait Paget's disease
Title Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone
Risk Allele A
P-val 2E-11
Odds Ratio 1.46 [1.30-1.63]