rs751828470
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs751828470(A;A) |
| Make rs751828470(A;C) |
| Make rs751828470(C;C) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 1 |
| Position | 45511415 |
| Gene | MMACHC, PRDX1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs751828470 |
| dbSNP (classic) | rs751828470 |
| ClinGen | rs751828470 |
| ebi | rs751828470 |
| HLI | rs751828470 |
| Exac | rs751828470 |
| Gnomad | rs751828470 |
| Varsome | rs751828470 |
| LitVar | rs751828470 |
| Map | rs751828470 |
| PheGenI | rs751828470 |
| Biobank | rs751828470 |
| 1000 genomes | rs751828470 |
| hgdp | rs751828470 |
| ensembl | rs751828470 |
| geneview | rs751828470 |
| scholar | rs751828470 |
| rs751828470 | |
| pharmgkb | rs751828470 |
| gwascentral | rs751828470 |
| openSNP | rs751828470 |
| 23andMe | rs751828470 |
| SNPshot | rs751828470 |
| SNPdbe | rs751828470 |
| MSV3d | rs751828470 |
| GWAS Ctlg | rs751828470 |
| Max Magnitude | 0 |
aka NM_181697.2(PRDX1):c.515-1G>T
OMIM pathogenic variant
