rs753966933
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs753966933(A;A) |
| Make rs753966933(A;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 15 |
| Position | 55228708 |
| Gene | RAB27A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs753966933 |
| dbSNP (classic) | rs753966933 |
| ClinGen | rs753966933 |
| ebi | rs753966933 |
| HLI | rs753966933 |
| Exac | rs753966933 |
| Gnomad | rs753966933 |
| Varsome | rs753966933 |
| LitVar | rs753966933 |
| Map | rs753966933 |
| PheGenI | rs753966933 |
| Biobank | rs753966933 |
| 1000 genomes | rs753966933 |
| hgdp | rs753966933 |
| ensembl | rs753966933 |
| geneview | rs753966933 |
| scholar | rs753966933 |
| rs753966933 | |
| pharmgkb | rs753966933 |
| gwascentral | rs753966933 |
| openSNP | rs753966933 |
| 23andMe | rs753966933 |
| SNPshot | rs753966933 |
| SNPdbe | rs753966933 |
| MSV3d | rs753966933 |
| GWAS Ctlg | rs753966933 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs753966933(A;A) |
| Alt | rs753966933(A;A) |
| Reference | Rs753966933(G;G) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | RAB27A |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000015.9:g.55520906G>A |
| CLNSRC | |
| CLNACC | RCV000483557.1, |
