rs137929776
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs137929776(C;T) |
| Make rs137929776(T;T) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 1 |
| Position | 151018530 |
| Gene | PRUNE, PRUNE1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs137929776 |
| dbSNP (classic) | rs137929776 |
| ClinGen | rs137929776 |
| ebi | rs137929776 |
| HLI | rs137929776 |
| Exac | rs137929776 |
| Gnomad | rs137929776 |
| Varsome | rs137929776 |
| LitVar | rs137929776 |
| Map | rs137929776 |
| PheGenI | rs137929776 |
| Biobank | rs137929776 |
| 1000 genomes | rs137929776 |
| hgdp | rs137929776 |
| ensembl | rs137929776 |
| geneview | rs137929776 |
| scholar | rs137929776 |
| rs137929776 | |
| pharmgkb | rs137929776 |
| gwascentral | rs137929776 |
| openSNP | rs137929776 |
| 23andMe | rs137929776 |
| SNPshot | rs137929776 |
| SNPdbe | rs137929776 |
| MSV3d | rs137929776 |
| GWAS Ctlg | rs137929776 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs137929776(T;T) |
| Alt | rs137929776(T;T) |
| Reference | Rs137929776(C;C) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | PRUNE PRUNE1 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000001.10:g.150991006C>T |
| CLNSRC | |
| CLNACC | RCV000492835.1, |
