rs774835569
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs774835569(C;C) |
| Make rs774835569(C;T) |
| Make rs774835569(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 16 |
| Position | 85918486 |
| Gene | IRF8, MIR6774 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs774835569 |
| dbSNP (classic) | rs774835569 |
| ClinGen | rs774835569 |
| ebi | rs774835569 |
| HLI | rs774835569 |
| Exac | rs774835569 |
| Gnomad | rs774835569 |
| Varsome | rs774835569 |
| LitVar | rs774835569 |
| Map | rs774835569 |
| PheGenI | rs774835569 |
| Biobank | rs774835569 |
| 1000 genomes | rs774835569 |
| hgdp | rs774835569 |
| ensembl | rs774835569 |
| geneview | rs774835569 |
| scholar | rs774835569 |
| rs774835569 | |
| pharmgkb | rs774835569 |
| gwascentral | rs774835569 |
| openSNP | rs774835569 |
| 23andMe | rs774835569 |
| SNPshot | rs774835569 |
| SNPdbe | rs774835569 |
| MSV3d | rs774835569 |
| GWAS Ctlg | rs774835569 |
| Max Magnitude | 0 |
aka NM_002163.2(IRF8):c.671C>T or (p.Pro224Leu)
OMIM pathogenic variant
