rs768607170
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs768607170(-;-) |
| Make rs768607170(-;G) |
| Make rs768607170(G;G) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 10 |
| Position | 100749771 |
| Gene | PAX2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs768607170 |
| dbSNP (classic) | rs768607170 |
| ClinGen | rs768607170 |
| ebi | rs768607170 |
| HLI | rs768607170 |
| Exac | rs768607170 |
| Gnomad | rs768607170 |
| Varsome | rs768607170 |
| LitVar | rs768607170 |
| Map | rs768607170 |
| PheGenI | rs768607170 |
| Biobank | rs768607170 |
| 1000 genomes | rs768607170 |
| hgdp | rs768607170 |
| ensembl | rs768607170 |
| geneview | rs768607170 |
| scholar | rs768607170 |
| rs768607170 | |
| pharmgkb | rs768607170 |
| gwascentral | rs768607170 |
| openSNP | rs768607170 |
| 23andMe | rs768607170 |
| SNPshot | rs768607170 |
| SNPdbe | rs768607170 |
| MSV3d | rs768607170 |
| GWAS Ctlg | rs768607170 |
| Max Magnitude | 0 |
aka NM_003990.4(PAX2):c.76dupG or (p.Val26Glyfs)
OMIM pathogenic variant
