rs75399846
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs75399846(C;C) |
| Make rs75399846(C;T) |
| Make rs75399846(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 10 |
| Position | 100806519 |
| Gene | PAX2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs75399846 |
| dbSNP (classic) | rs75399846 |
| ClinGen | rs75399846 |
| ebi | rs75399846 |
| HLI | rs75399846 |
| Exac | rs75399846 |
| Gnomad | rs75399846 |
| Varsome | rs75399846 |
| LitVar | rs75399846 |
| Map | rs75399846 |
| PheGenI | rs75399846 |
| Biobank | rs75399846 |
| 1000 genomes | rs75399846 |
| hgdp | rs75399846 |
| ensembl | rs75399846 |
| geneview | rs75399846 |
| scholar | rs75399846 |
| rs75399846 | |
| pharmgkb | rs75399846 |
| gwascentral | rs75399846 |
| openSNP | rs75399846 |
| 23andMe | rs75399846 |
| SNPshot | rs75399846 |
| SNPdbe | rs75399846 |
| MSV3d | rs75399846 |
| GWAS Ctlg | rs75399846 |
| Max Magnitude | 0 |
aka NM_000278.4(PAX2):c.706C>T or (p.Gln236Ter)
OMIM pathogenic variant
