rs202059967
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs202059967(A;A) |
| Make rs202059967(A;C) |
| Make rs202059967(C;C) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 22 |
| Position | 19878372 |
| Gene | TXNRD2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs202059967 |
| dbSNP (classic) | rs202059967 |
| ClinGen | rs202059967 |
| ebi | rs202059967 |
| HLI | rs202059967 |
| Exac | rs202059967 |
| Gnomad | rs202059967 |
| Varsome | rs202059967 |
| LitVar | rs202059967 |
| Map | rs202059967 |
| PheGenI | rs202059967 |
| Biobank | rs202059967 |
| 1000 genomes | rs202059967 |
| hgdp | rs202059967 |
| ensembl | rs202059967 |
| geneview | rs202059967 |
| scholar | rs202059967 |
| rs202059967 | |
| pharmgkb | rs202059967 |
| gwascentral | rs202059967 |
| openSNP | rs202059967 |
| 23andMe | rs202059967 |
| SNPshot | rs202059967 |
| SNPdbe | rs202059967 |
| MSV3d | rs202059967 |
| GWAS Ctlg | rs202059967 |
| Max Magnitude | 0 |
OMIM pathogenic variant
