rs794729032
From SNPedia
| Merged into | rs782392706 |
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs794729032(C;C) |
| Make rs794729032(C;G) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 17 |
| Position | 41769480 |
| Gene | JUP |
| is a | snp |
| is | mentioned by |
| dbSNP | rs794729032 |
| dbSNP (classic) | rs794729032 |
| ClinGen | rs794729032 |
| ebi | rs794729032 |
| HLI | rs794729032 |
| Exac | rs794729032 |
| Gnomad | rs794729032 |
| Varsome | rs794729032 |
| LitVar | rs794729032 |
| Map | rs794729032 |
| PheGenI | rs794729032 |
| Biobank | rs794729032 |
| 1000 genomes | rs794729032 |
| hgdp | rs794729032 |
| ensembl | rs794729032 |
| geneview | rs794729032 |
| scholar | rs794729032 |
| rs794729032 | |
| pharmgkb | rs794729032 |
| gwascentral | rs794729032 |
| openSNP | rs794729032 |
| 23andMe | rs794729032 |
| SNPshot | rs794729032 |
| SNPdbe | rs794729032 |
| MSV3d | rs794729032 |
| GWAS Ctlg | rs794729032 |
| Status | Merged into rs782392706 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs794729032(C;C) |
| Alt | rs794729032(C;C) |
| Reference | Rs794729032(G;G) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | JUP |
| CLNDBN | not provided |
| Reversed | 1 |
| HGVS | NC_000017.10:g.39925732C>G |
| CLNSRC | |
| CLNACC | RCV000183484.2, |
