rs200449378
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs200449378(C;C) |
| Make rs200449378(C;T) |
| Make rs200449378(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 11 |
| Position | 18310943 |
| Gene | HPS5 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs200449378 |
| dbSNP (classic) | rs200449378 |
| ClinGen | rs200449378 |
| ebi | rs200449378 |
| HLI | rs200449378 |
| Exac | rs200449378 |
| Gnomad | rs200449378 |
| Varsome | rs200449378 |
| LitVar | rs200449378 |
| Map | rs200449378 |
| PheGenI | rs200449378 |
| Biobank | rs200449378 |
| 1000 genomes | rs200449378 |
| hgdp | rs200449378 |
| ensembl | rs200449378 |
| geneview | rs200449378 |
| scholar | rs200449378 |
| rs200449378 | |
| pharmgkb | rs200449378 |
| gwascentral | rs200449378 |
| openSNP | rs200449378 |
| 23andMe | rs200449378 |
| SNPshot | rs200449378 |
| SNPdbe | rs200449378 |
| MSV3d | rs200449378 |
| GWAS Ctlg | rs200449378 |
| Max Magnitude | 0 |
OMIM pathogenic variant
