rs376589026
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs376589026(G;T) |
| Make rs376589026(T;T) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 3 |
| Position | 14139302 |
| Gene | TMEM43 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs376589026 |
| dbSNP (classic) | rs376589026 |
| ClinGen | rs376589026 |
| ebi | rs376589026 |
| HLI | rs376589026 |
| Exac | rs376589026 |
| Gnomad | rs376589026 |
| Varsome | rs376589026 |
| LitVar | rs376589026 |
| Map | rs376589026 |
| PheGenI | rs376589026 |
| Biobank | rs376589026 |
| 1000 genomes | rs376589026 |
| hgdp | rs376589026 |
| ensembl | rs376589026 |
| geneview | rs376589026 |
| scholar | rs376589026 |
| rs376589026 | |
| pharmgkb | rs376589026 |
| gwascentral | rs376589026 |
| openSNP | rs376589026 |
| 23andMe | rs376589026 |
| SNPshot | rs376589026 |
| SNPdbe | rs376589026 |
| MSV3d | rs376589026 |
| GWAS Ctlg | rs376589026 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs376589026(T;T) |
| Alt | rs376589026(T;T) |
| Reference | Rs376589026(G;G) |
| Significance | Probable-Pathogenic |
| Disease | not specified |
| Variation | info |
| Gene | TMEM43 |
| CLNDBN | not specified |
| Reversed | 0 |
| HGVS | NC_000003.11:g.14180802G>T |
| CLNSRC | |
| CLNACC | RCV000039374.2, |
