rs80356379
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (;) | 0 | common in clinvar |
| (-;-) | 0 | common in complete genomics |
| Make rs80356379(-;CGGCAG) |
| Make rs80356379(CGGCAG;CGGCAG) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 10 |
| Position | 100750712 |
| Gene | PAX2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs80356379 |
| dbSNP (classic) | rs80356379 |
| ClinGen | rs80356379 |
| ebi | rs80356379 |
| HLI | rs80356379 |
| Exac | rs80356379 |
| Gnomad | rs80356379 |
| Varsome | rs80356379 |
| LitVar | rs80356379 |
| Map | rs80356379 |
| PheGenI | rs80356379 |
| Biobank | rs80356379 |
| 1000 genomes | rs80356379 |
| hgdp | rs80356379 |
| ensembl | rs80356379 |
| geneview | rs80356379 |
| scholar | rs80356379 |
| rs80356379 | |
| pharmgkb | rs80356379 |
| gwascentral | rs80356379 |
| openSNP | rs80356379 |
| 23andMe | rs80356379 |
| SNPshot | rs80356379 |
| SNPdbe | rs80356379 |
| MSV3d | rs80356379 |
| GWAS Ctlg | rs80356379 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs80356379(CGGCAG;CGGCAG) |
| Alt | rs80356379(CGGCAG;CGGCAG) |
| Reference | Rs80356379(-;-) |
| Significance | Untested |
| Disease | not provided |
| Variation | info |
| Gene | PAX2 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000010.10:g.102510469_102510470insCGGCAG |
| CLNSRC | ClinVar |
| CLNACC | RCV000144375.1, |
