rs753034799
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs753034799(C;C) |
| Make rs753034799(C;T) |
| Make rs753034799(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 10 |
| Position | 101022246 |
| Gene | PDZD7 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs753034799 |
| dbSNP (classic) | rs753034799 |
| ClinGen | rs753034799 |
| ebi | rs753034799 |
| HLI | rs753034799 |
| Exac | rs753034799 |
| Gnomad | rs753034799 |
| Varsome | rs753034799 |
| LitVar | rs753034799 |
| Map | rs753034799 |
| PheGenI | rs753034799 |
| Biobank | rs753034799 |
| 1000 genomes | rs753034799 |
| hgdp | rs753034799 |
| ensembl | rs753034799 |
| geneview | rs753034799 |
| scholar | rs753034799 |
| rs753034799 | |
| pharmgkb | rs753034799 |
| gwascentral | rs753034799 |
| openSNP | rs753034799 |
| 23andMe | rs753034799 |
| SNPshot | rs753034799 |
| SNPdbe | rs753034799 |
| MSV3d | rs753034799 |
| GWAS Ctlg | rs753034799 |
| Max Magnitude | 0 |
aka NM_001195263.1(PDZD7):c.682G>A or (p.Gly228Arg)
OMIM pathogenic variant
