rs139805921
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs139805921(A;A) |
| Make rs139805921(A;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 21 |
| Position | 42388935 |
| Gene | TMPRSS3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs139805921 |
| dbSNP (classic) | rs139805921 |
| ClinGen | rs139805921 |
| ebi | rs139805921 |
| HLI | rs139805921 |
| Exac | rs139805921 |
| Gnomad | rs139805921 |
| Varsome | rs139805921 |
| LitVar | rs139805921 |
| Map | rs139805921 |
| PheGenI | rs139805921 |
| Biobank | rs139805921 |
| 1000 genomes | rs139805921 |
| hgdp | rs139805921 |
| ensembl | rs139805921 |
| geneview | rs139805921 |
| scholar | rs139805921 |
| rs139805921 | |
| pharmgkb | rs139805921 |
| gwascentral | rs139805921 |
| openSNP | rs139805921 |
| 23andMe | rs139805921 |
| SNPshot | rs139805921 |
| SNPdbe | rs139805921 |
| MSV3d | rs139805921 |
| GWAS Ctlg | rs139805921 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs139805921(A;A) |
| Alt | rs139805921(A;A) |
| Reference | Rs139805921(G;G) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | TMPRSS3 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000021.8:g.43809044G>A |
| CLNSRC | |
| CLNACC | RCV000441150.1, |
