rs879253863
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs879253863(A;C) |
| Make rs879253863(C;C) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 4 |
| Position | 153324126 |
| Gene | TRIM2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs879253863 |
| dbSNP (classic) | rs879253863 |
| ClinGen | rs879253863 |
| ebi | rs879253863 |
| HLI | rs879253863 |
| Exac | rs879253863 |
| Gnomad | rs879253863 |
| Varsome | rs879253863 |
| LitVar | rs879253863 |
| Map | rs879253863 |
| PheGenI | rs879253863 |
| Biobank | rs879253863 |
| 1000 genomes | rs879253863 |
| hgdp | rs879253863 |
| ensembl | rs879253863 |
| geneview | rs879253863 |
| scholar | rs879253863 |
| rs879253863 | |
| pharmgkb | rs879253863 |
| gwascentral | rs879253863 |
| openSNP | rs879253863 |
| 23andMe | rs879253863 |
| SNPshot | rs879253863 |
| SNPdbe | rs879253863 |
| MSV3d | rs879253863 |
| GWAS Ctlg | rs879253863 |
| Max Magnitude | 0 |
aka NM_015271.4(TRIM2):c.2000A>C or (p.Asp667Ala)
OMIM pathogenic variant
