rs7795356
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7795356(C;C) |
| Make rs7795356(C;T) |
| Make rs7795356(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 116576975 |
| Gene | LINC01510 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7795356 |
| dbSNP (classic) | rs7795356 |
| ClinGen | rs7795356 |
| ebi | rs7795356 |
| HLI | rs7795356 |
| Exac | rs7795356 |
| Gnomad | rs7795356 |
| Varsome | rs7795356 |
| LitVar | rs7795356 |
| Map | rs7795356 |
| PheGenI | rs7795356 |
| Biobank | rs7795356 |
| 1000 genomes | rs7795356 |
| hgdp | rs7795356 |
| ensembl | rs7795356 |
| geneview | rs7795356 |
| scholar | rs7795356 |
| rs7795356 | |
| pharmgkb | rs7795356 |
| gwascentral | rs7795356 |
| openSNP | rs7795356 |
| 23andMe | rs7795356 |
| SNPshot | rs7795356 |
| SNPdbe | rs7795356 |
| MSV3d | rs7795356 |
| GWAS Ctlg | rs7795356 |
| GMAF | 0.1777 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 23743525
] Association study of genetic variants on chromosome 7q31 with susceptibility to normal tension glaucoma in a Japanese population
