rs931317
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs931317(A;A) |
Make rs931317(A;G) |
Make rs931317(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 59943125 |
Gene | FHIT |
is a | snp |
is | mentioned by |
dbSNP | rs931317 |
dbSNP (classic) | rs931317 |
ClinGen | rs931317 |
ebi | rs931317 |
HLI | rs931317 |
Exac | rs931317 |
Gnomad | rs931317 |
Varsome | rs931317 |
LitVar | rs931317 |
Map | rs931317 |
PheGenI | rs931317 |
Biobank | rs931317 |
1000 genomes | rs931317 |
hgdp | rs931317 |
ensembl | rs931317 |
geneview | rs931317 |
scholar | rs931317 |
rs931317 | |
pharmgkb | rs931317 |
gwascentral | rs931317 |
openSNP | rs931317 |
23andMe | rs931317 |
SNPshot | rs931317 |
SNPdbe | rs931317 |
MSV3d | rs931317 |
GWAS Ctlg | rs931317 |
GMAF | 0.1726 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 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 | 3E-6 |
Odds Ratio | NR NR |