rs1052990
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1052990(G;G) |
| Make rs1052990(G;T) |
| Make rs1052990(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 116508316 |
| Gene | CAV2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1052990 |
| dbSNP (classic) | rs1052990 |
| ClinGen | rs1052990 |
| ebi | rs1052990 |
| HLI | rs1052990 |
| Exac | rs1052990 |
| Gnomad | rs1052990 |
| Varsome | rs1052990 |
| LitVar | rs1052990 |
| Map | rs1052990 |
| PheGenI | rs1052990 |
| Biobank | rs1052990 |
| 1000 genomes | rs1052990 |
| hgdp | rs1052990 |
| ensembl | rs1052990 |
| geneview | rs1052990 |
| scholar | rs1052990 |
| rs1052990 | |
| pharmgkb | rs1052990 |
| gwascentral | rs1052990 |
| openSNP | rs1052990 |
| 23andMe | rs1052990 |
| SNPshot | rs1052990 |
| SNPdbe | rs1052990 |
| MSV3d | rs1052990 |
| GWAS Ctlg | rs1052990 |
| GMAF | 0.3113 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 23743525
] Association study of genetic variants on chromosome 7q31 with susceptibility to normal tension glaucoma in a Japanese population
[PMID 26015768] Expression-associated polymorphisms of CAV1-CAV2 affect intraocular pressure and high-tension glaucoma risk
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 7
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip NatGeo2
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
