rs923375
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs923375(C;C) |
Make rs923375(C;T) |
Make rs923375(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 3489774 |
Gene | ASPA, SPATA22 |
is a | snp |
is | mentioned by |
dbSNP | rs923375 |
dbSNP (classic) | rs923375 |
ClinGen | rs923375 |
ebi | rs923375 |
HLI | rs923375 |
Exac | rs923375 |
Gnomad | rs923375 |
Varsome | rs923375 |
LitVar | rs923375 |
Map | rs923375 |
PheGenI | rs923375 |
Biobank | rs923375 |
1000 genomes | rs923375 |
hgdp | rs923375 |
ensembl | rs923375 |
geneview | rs923375 |
scholar | rs923375 |
rs923375 | |
pharmgkb | rs923375 |
gwascentral | rs923375 |
openSNP | rs923375 |
23andMe | rs923375 |
SNPshot | rs923375 |
SNPdbe | rs923375 |
MSV3d | rs923375 |
GWAS Ctlg | rs923375 |
GMAF | 0.2594 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23049088] |
Trait | Myopia (pathological) |
Title | A Genome-Wide Association Study Provides Evidence for Association of Chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with High Myopia in the French Population. |
Risk Allele | |
P-val | 4E-16 |
Odds Ratio | NR NR |