rs10494112
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10494112(A;A) |
Make rs10494112(A;G) |
Make rs10494112(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 109809855 |
is a | snp |
is | mentioned by |
dbSNP | rs10494112 |
dbSNP (classic) | rs10494112 |
ClinGen | rs10494112 |
ebi | rs10494112 |
HLI | rs10494112 |
Exac | rs10494112 |
Gnomad | rs10494112 |
Varsome | rs10494112 |
LitVar | rs10494112 |
Map | rs10494112 |
PheGenI | rs10494112 |
Biobank | rs10494112 |
1000 genomes | rs10494112 |
hgdp | rs10494112 |
ensembl | rs10494112 |
geneview | rs10494112 |
scholar | rs10494112 |
rs10494112 | |
pharmgkb | rs10494112 |
gwascentral | rs10494112 |
openSNP | rs10494112 |
23andMe | rs10494112 |
SNPshot | rs10494112 |
SNPdbe | rs10494112 |
MSV3d | rs10494112 |
GWAS Ctlg | rs10494112 |
GMAF | 0.1244 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
related to Paget’s disease of bone 23andMe blog.
GWAS snp | |
---|---|
PMID | [PMID 21623375] |
Trait | |
Title | Genome-wide association identifies three new susceptibility loci for Paget's disease of bone. |
Risk Allele | G |
P-val | 7E-35 |
Odds Ratio | 1.7200 [1.57-1.87] |