rs10809650
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10809650(A;A) |
Make rs10809650(A;G) |
Make rs10809650(G;G) |
Reference | GRCh37.p5 37.3/137 |
Chromosome | 9 |
Position | 1202371 |
is a | snp |
is | mentioned by |
dbSNP | rs10809650 |
dbSNP (classic) | rs10809650 |
ClinGen | rs10809650 |
ebi | rs10809650 |
HLI | rs10809650 |
Exac | rs10809650 |
Gnomad | rs10809650 |
Varsome | rs10809650 |
LitVar | rs10809650 |
Map | rs10809650 |
PheGenI | rs10809650 |
Biobank | rs10809650 |
1000 genomes | rs10809650 |
hgdp | rs10809650 |
ensembl | rs10809650 |
geneview | rs10809650 |
scholar | rs10809650 |
rs10809650 | |
pharmgkb | rs10809650 |
gwascentral | rs10809650 |
openSNP | rs10809650 |
23andMe | rs10809650 |
SNPshot | rs10809650 |
SNPdbe | rs10809650 |
MSV3d | rs10809650 |
GWAS Ctlg | rs10809650 |
GMAF | 0.3292 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21732829] |
Trait | |
Title | Wnt signaling and Dupuytren's disease. |
Risk Allele | |
P-val | 6E-9 |
Odds Ratio | 1.2500 None |