rs10902758
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| (G;G) | 0 | common in clinvar |
| Make rs10902758(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 654854 |
| Gene | LOC101928521, PDE6B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10902758 |
| dbSNP (classic) | rs10902758 |
| ClinGen | rs10902758 |
| ebi | rs10902758 |
| HLI | rs10902758 |
| Exac | rs10902758 |
| Gnomad | rs10902758 |
| Varsome | rs10902758 |
| LitVar | rs10902758 |
| Map | rs10902758 |
| PheGenI | rs10902758 |
| Biobank | rs10902758 |
| 1000 genomes | rs10902758 |
| hgdp | rs10902758 |
| ensembl | rs10902758 |
| geneview | rs10902758 |
| scholar | rs10902758 |
| rs10902758 | |
| pharmgkb | rs10902758 |
| gwascentral | rs10902758 |
| openSNP | rs10902758 |
| 23andMe | rs10902758 |
| SNPshot | rs10902758 |
| SNPdbe | rs10902758 |
| MSV3d | rs10902758 |
| GWAS Ctlg | rs10902758 |
| GMAF | 0.0005 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 19339744
] Genetic analysis of Indian families with autosomal recessive retinitis pigmentosa by homozygosity screening.
| ClinVar | |
|---|---|
| Risk | Rs10902758(A;A) |
| Alt | Rs10902758(A;A) |
| Reference | Rs10902758(G;G) |
| Significance | Non-pathogenic |
| Disease | not specified |
| Variation | info |
| Gene | PDE6B RP11-1191J2.2 |
| CLNDBN | not specified |
| Reversed | 0 |
| HGVS | NC_000004.11:g.648643G>A |
| CLNSRC | |
| CLNACC | RCV000153663.3, |
