rs2957128
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2957128(A;A) |
Make rs2957128(A;G) |
Make rs2957128(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 18 |
Position | 62393502 |
is a | snp |
is | mentioned by |
dbSNP | rs2957128 |
dbSNP (classic) | rs2957128 |
ClinGen | rs2957128 |
ebi | rs2957128 |
HLI | rs2957128 |
Exac | rs2957128 |
Gnomad | rs2957128 |
Varsome | rs2957128 |
LitVar | rs2957128 |
Map | rs2957128 |
PheGenI | rs2957128 |
Biobank | rs2957128 |
1000 genomes | rs2957128 |
hgdp | rs2957128 |
ensembl | rs2957128 |
geneview | rs2957128 |
scholar | rs2957128 |
rs2957128 | |
pharmgkb | rs2957128 |
gwascentral | rs2957128 |
openSNP | rs2957128 |
23andMe | rs2957128 |
SNPshot | rs2957128 |
SNPdbe | rs2957128 |
MSV3d | rs2957128 |
GWAS Ctlg | rs2957128 |
GMAF | 0.4848 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
related to Paget’s disease of bone 23andMe blog.
GWAS snp | |
---|---|
PMID | [PMID 20436471] |
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] |