rs80356760
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (-;-) | 0 | common in clinvar |
| (ACT;ACT) | 0 | common in clinvar |
| (TCA;TCA) | 0 | common in clinvar |
| Make rs80356760(-;G) |
| Make rs80356760(G;G) |
| Reference | GRCh37.p5 37.3/137 |
| Chromosome | 1 |
| Position | 155240651 |
| Gene | GBA |
| is a | snp |
| is | mentioned by |
| dbSNP | rs80356760 |
| dbSNP (classic) | rs80356760 |
| ClinGen | rs80356760 |
| ebi | rs80356760 |
| HLI | rs80356760 |
| Exac | rs80356760 |
| Gnomad | rs80356760 |
| Varsome | rs80356760 |
| LitVar | rs80356760 |
| Map | rs80356760 |
| PheGenI | rs80356760 |
| Biobank | rs80356760 |
| 1000 genomes | rs80356760 |
| hgdp | rs80356760 |
| ensembl | rs80356760 |
| geneview | rs80356760 |
| scholar | rs80356760 |
| rs80356760 | |
| pharmgkb | rs80356760 |
| gwascentral | rs80356760 |
| openSNP | rs80356760 |
| 23andMe | rs80356760 |
| SNPshot | rs80356760 |
| SNPdbe | rs80356760 |
| MSV3d | rs80356760 |
| GWAS Ctlg | rs80356760 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs80356760(G;G) |
| Alt | rs80356760(G;G) |
| Reference | Rs80356760(-;-) |
| Significance | Pathogenic |
| Disease | Gaucher disease |
| Variation | info |
| Gene | GBA |
| CLNDBN | Gaucher disease |
| Reversed | 1 |
| HGVS | NC_000001.10:g.155210442_155210443insC |
| CLNSRC | ClinVar GeneReviews |
| CLNACC | RCV000020160.1, |
