rs953422571
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs953422571(A;A) |
| Make rs953422571(A;G) |
| Make rs953422571(G;G) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 10 |
| Position | 101018121 |
| Gene | PDZD7 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs953422571 |
| dbSNP (classic) | rs953422571 |
| ClinGen | rs953422571 |
| ebi | rs953422571 |
| HLI | rs953422571 |
| Exac | rs953422571 |
| Gnomad | rs953422571 |
| Varsome | rs953422571 |
| LitVar | rs953422571 |
| Map | rs953422571 |
| PheGenI | rs953422571 |
| Biobank | rs953422571 |
| 1000 genomes | rs953422571 |
| hgdp | rs953422571 |
| ensembl | rs953422571 |
| geneview | rs953422571 |
| scholar | rs953422571 |
| rs953422571 | |
| pharmgkb | rs953422571 |
| gwascentral | rs953422571 |
| openSNP | rs953422571 |
| 23andMe | rs953422571 |
| SNPshot | rs953422571 |
| SNPdbe | rs953422571 |
| MSV3d | rs953422571 |
| GWAS Ctlg | rs953422571 |
| Max Magnitude | 0 |
aka NM_001351044.1(PDZD7):c.1528C>A or (p.Pro510Thr)
OMIM pathogenic variant
