rs139484231
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs139484231(C;T) |
| Make rs139484231(T;T) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 21 |
| Position | 42388523 |
| Gene | TMPRSS3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs139484231 |
| dbSNP (classic) | rs139484231 |
| ClinGen | rs139484231 |
| ebi | rs139484231 |
| HLI | rs139484231 |
| Exac | rs139484231 |
| Gnomad | rs139484231 |
| Varsome | rs139484231 |
| LitVar | rs139484231 |
| Map | rs139484231 |
| PheGenI | rs139484231 |
| Biobank | rs139484231 |
| 1000 genomes | rs139484231 |
| hgdp | rs139484231 |
| ensembl | rs139484231 |
| geneview | rs139484231 |
| scholar | rs139484231 |
| rs139484231 | |
| pharmgkb | rs139484231 |
| gwascentral | rs139484231 |
| openSNP | rs139484231 |
| 23andMe | rs139484231 |
| SNPshot | rs139484231 |
| SNPdbe | rs139484231 |
| MSV3d | rs139484231 |
| GWAS Ctlg | rs139484231 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs139484231(T;T) |
| Alt | rs139484231(T;T) |
| Reference | Rs139484231(C;C) |
| Significance | Probable-Pathogenic |
| Disease | not specified not provided |
| Variation | info |
| Gene | TMPRSS3 |
| CLNDBN | not specified not provided |
| Reversed | 0 |
| HGVS | NC_000021.8:g.43808632C>T |
| CLNSRC | |
| CLNACC | RCV000178994.1, RCV000493533.1, |
