rs369586696
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Make rs369586696(A;G) |
| Make rs369586696(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 101421877 |
| Gene | ALDOB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs369586696 |
| dbSNP (classic) | rs369586696 |
| ClinGen | rs369586696 |
| ebi | rs369586696 |
| HLI | rs369586696 |
| Exac | rs369586696 |
| Gnomad | rs369586696 |
| Varsome | rs369586696 |
| LitVar | rs369586696 |
| Map | rs369586696 |
| PheGenI | rs369586696 |
| Biobank | rs369586696 |
| 1000 genomes | rs369586696 |
| hgdp | rs369586696 |
| ensembl | rs369586696 |
| geneview | rs369586696 |
| scholar | rs369586696 |
| rs369586696 | |
| pharmgkb | rs369586696 |
| gwascentral | rs369586696 |
| openSNP | rs369586696 |
| 23andMe | rs369586696 |
| SNPshot | rs369586696 |
| SNPdbe | rs369586696 |
| MSV3d | rs369586696 |
| GWAS Ctlg | rs369586696 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs369586696(G;G) |
| Alt | rs369586696(G;G) |
| Reference | Rs369586696(A;A) |
| Significance | Pathogenic |
| Disease | Hereditary fructosuria |
| Variation | info |
| Gene | ALDOB |
| CLNDBN | Hereditary fructosuria |
| Reversed | 0 |
| HGVS | NC_000009.11:g.104184159A>G |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000023971.3, |
