rs4149311
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs4149311(A;A) |
Make rs4149311(A;G) |
Make rs4149311(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 104826496 |
Gene | ABCA1 |
is a | snp |
is | mentioned by |
dbSNP | rs4149311 |
dbSNP (classic) | rs4149311 |
ClinGen | rs4149311 |
ebi | rs4149311 |
HLI | rs4149311 |
Exac | rs4149311 |
Gnomad | rs4149311 |
Varsome | rs4149311 |
LitVar | rs4149311 |
Map | rs4149311 |
PheGenI | rs4149311 |
Biobank | rs4149311 |
1000 genomes | rs4149311 |
hgdp | rs4149311 |
ensembl | rs4149311 |
geneview | rs4149311 |
scholar | rs4149311 |
rs4149311 | |
pharmgkb | rs4149311 |
gwascentral | rs4149311 |
openSNP | rs4149311 |
23andMe | rs4149311 |
SNPshot | rs4149311 |
SNPdbe | rs4149311 |
MSV3d | rs4149311 |
GWAS Ctlg | rs4149311 |
GMAF | 0.3512 |
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 | 9E-6 |
Odds Ratio | NR NR |