rs13172324
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common genotype |
Make rs13172324(C;T) |
Make rs13172324(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 7368732 |
Gene | LOC105374645 |
is a | snp |
is | mentioned by |
dbSNP | rs13172324 |
dbSNP (classic) | rs13172324 |
ClinGen | rs13172324 |
ebi | rs13172324 |
HLI | rs13172324 |
Exac | rs13172324 |
Gnomad | rs13172324 |
Varsome | rs13172324 |
LitVar | rs13172324 |
Map | rs13172324 |
PheGenI | rs13172324 |
Biobank | rs13172324 |
1000 genomes | rs13172324 |
hgdp | rs13172324 |
ensembl | rs13172324 |
geneview | rs13172324 |
scholar | rs13172324 |
rs13172324 | |
pharmgkb | rs13172324 |
gwascentral | rs13172324 |
openSNP | rs13172324 |
23andMe | rs13172324 |
SNPshot | rs13172324 |
SNPdbe | rs13172324 |
MSV3d | rs13172324 |
GWAS Ctlg | rs13172324 |
GMAF | 0.03673 |
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 | 3E-10 |
Odds Ratio | NR NR |