rs148695069
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs148695069(C;C) |
| Make rs148695069(C;G) |
| Make rs148695069(G;G) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 10 |
| Position | 101023988 |
| Gene | PDZD7 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs148695069 |
| dbSNP (classic) | rs148695069 |
| ClinGen | rs148695069 |
| ebi | rs148695069 |
| HLI | rs148695069 |
| Exac | rs148695069 |
| Gnomad | rs148695069 |
| Varsome | rs148695069 |
| LitVar | rs148695069 |
| Map | rs148695069 |
| PheGenI | rs148695069 |
| Biobank | rs148695069 |
| 1000 genomes | rs148695069 |
| hgdp | rs148695069 |
| ensembl | rs148695069 |
| geneview | rs148695069 |
| scholar | rs148695069 |
| rs148695069 | |
| pharmgkb | rs148695069 |
| gwascentral | rs148695069 |
| openSNP | rs148695069 |
| 23andMe | rs148695069 |
| SNPshot | rs148695069 |
| SNPdbe | rs148695069 |
| MSV3d | rs148695069 |
| GWAS Ctlg | rs148695069 |
| Max Magnitude | 0 |
OMIM pathogenic variant
