rs11838472
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11838472(C;C) |
| Make rs11838472(C;T) |
| Make rs11838472(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 13 |
| Position | 73167012 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11838472 |
| dbSNP (classic) | rs11838472 |
| ClinGen | rs11838472 |
| ebi | rs11838472 |
| HLI | rs11838472 |
| Exac | rs11838472 |
| Gnomad | rs11838472 |
| Varsome | rs11838472 |
| LitVar | rs11838472 |
| Map | rs11838472 |
| PheGenI | rs11838472 |
| Biobank | rs11838472 |
| 1000 genomes | rs11838472 |
| hgdp | rs11838472 |
| ensembl | rs11838472 |
| geneview | rs11838472 |
| scholar | rs11838472 |
| rs11838472 | |
| pharmgkb | rs11838472 |
| gwascentral | rs11838472 |
| openSNP | rs11838472 |
| 23andMe | rs11838472 |
| SNPshot | rs11838472 |
| SNPdbe | rs11838472 |
| MSV3d | rs11838472 |
| GWAS Ctlg | rs11838472 |
| GMAF | 0.1667 |
| 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-17 |
| Odds Ratio | NR NR |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 13
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip NatGeo2
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
