rs752283089
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs752283089(G;T) |
| Make rs752283089(T;T) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 14 |
| Position | 67783217 |
| Gene | ZFYVE26 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs752283089 |
| dbSNP (classic) | rs752283089 |
| ClinGen | rs752283089 |
| ebi | rs752283089 |
| HLI | rs752283089 |
| Exac | rs752283089 |
| Gnomad | rs752283089 |
| Varsome | rs752283089 |
| LitVar | rs752283089 |
| Map | rs752283089 |
| PheGenI | rs752283089 |
| Biobank | rs752283089 |
| 1000 genomes | rs752283089 |
| hgdp | rs752283089 |
| ensembl | rs752283089 |
| geneview | rs752283089 |
| scholar | rs752283089 |
| rs752283089 | |
| pharmgkb | rs752283089 |
| gwascentral | rs752283089 |
| openSNP | rs752283089 |
| 23andMe | rs752283089 |
| SNPshot | rs752283089 |
| SNPdbe | rs752283089 |
| MSV3d | rs752283089 |
| GWAS Ctlg | rs752283089 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs752283089(T;T) |
| Alt | rs752283089(T;T) |
| Reference | Rs752283089(G;G) |
| Significance | Pathogenic |
| Disease | Inborn genetic diseases |
| Variation | info |
| Gene | ZFYVE26 |
| CLNDBN | Inborn genetic diseases |
| Reversed | 0 |
| HGVS | NC_000014.8:g.68249934G>T |
| CLNSRC | |
| CLNACC | RCV000210539.1, |
