rs376882637
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs376882637(C;C) |
| Make rs376882637(C;G) |
| Make rs376882637(G;G) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 5 |
| Position | 914504 |
| Gene | TRIP13 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs376882637 |
| dbSNP (classic) | rs376882637 |
| ClinGen | rs376882637 |
| ebi | rs376882637 |
| HLI | rs376882637 |
| Exac | rs376882637 |
| Gnomad | rs376882637 |
| Varsome | rs376882637 |
| LitVar | rs376882637 |
| Map | rs376882637 |
| PheGenI | rs376882637 |
| Biobank | rs376882637 |
| 1000 genomes | rs376882637 |
| hgdp | rs376882637 |
| ensembl | rs376882637 |
| geneview | rs376882637 |
| scholar | rs376882637 |
| rs376882637 | |
| pharmgkb | rs376882637 |
| gwascentral | rs376882637 |
| openSNP | rs376882637 |
| 23andMe | rs376882637 |
| SNPshot | rs376882637 |
| SNPdbe | rs376882637 |
| MSV3d | rs376882637 |
| GWAS Ctlg | rs376882637 |
| Max Magnitude | 0 |
aka NM_004237.3(TRIP13):c.1060C>T or (p.Arg354Ter)
OMIM pathogenic variant
