rs142012387
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs142012387(G;T) |
| Make rs142012387(T;T) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 10 |
| Position | 70600460 |
| Gene | PRF1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs142012387 |
| dbSNP (classic) | rs142012387 |
| ClinGen | rs142012387 |
| ebi | rs142012387 |
| HLI | rs142012387 |
| Exac | rs142012387 |
| Gnomad | rs142012387 |
| Varsome | rs142012387 |
| LitVar | rs142012387 |
| Map | rs142012387 |
| PheGenI | rs142012387 |
| Biobank | rs142012387 |
| 1000 genomes | rs142012387 |
| hgdp | rs142012387 |
| ensembl | rs142012387 |
| geneview | rs142012387 |
| scholar | rs142012387 |
| rs142012387 | |
| pharmgkb | rs142012387 |
| gwascentral | rs142012387 |
| openSNP | rs142012387 |
| 23andMe | rs142012387 |
| SNPshot | rs142012387 |
| SNPdbe | rs142012387 |
| MSV3d | rs142012387 |
| GWAS Ctlg | rs142012387 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs142012387(C;C) rs142012387(T;T) |
| Alt | rs142012387(C;C) rs142012387(T;T) |
| Reference | Rs142012387(G;G) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | PRF1 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000010.10:g.72360216G>C |
| CLNSRC | |
| CLNACC | RCV000424261.1, |
