rs10490775
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common on affy axiom data |
Make rs10490775(A;A) |
Make rs10490775(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 62051050 |
Gene | PTPRG |
is a | snp |
is | mentioned by |
dbSNP | rs10490775 |
dbSNP (classic) | rs10490775 |
ClinGen | rs10490775 |
ebi | rs10490775 |
HLI | rs10490775 |
Exac | rs10490775 |
Gnomad | rs10490775 |
Varsome | rs10490775 |
LitVar | rs10490775 |
Map | rs10490775 |
PheGenI | rs10490775 |
Biobank | rs10490775 |
1000 genomes | rs10490775 |
hgdp | rs10490775 |
ensembl | rs10490775 |
geneview | rs10490775 |
scholar | rs10490775 |
rs10490775 | |
pharmgkb | rs10490775 |
gwascentral | rs10490775 |
openSNP | rs10490775 |
23andMe | rs10490775 |
SNPshot | rs10490775 |
SNPdbe | rs10490775 |
MSV3d | rs10490775 |
GWAS Ctlg | rs10490775 |
GMAF | 0.0854 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20825314] |
Trait | |
Title | E2-2 protein and Fuchs's corneal dystrophy |
Risk Allele | A |
P-val | 0.000001 |
Odds Ratio | 2.30 [1.64-3.22] |