rs148158093
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs148158093(A;A) |
| Make rs148158093(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | X |
| Position | 101403828 |
| Gene | GLA, RPL36A-HNRNPH2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs148158093 |
| dbSNP (classic) | rs148158093 |
| ClinGen | rs148158093 |
| ebi | rs148158093 |
| HLI | rs148158093 |
| Exac | rs148158093 |
| Gnomad | rs148158093 |
| Varsome | rs148158093 |
| LitVar | rs148158093 |
| Map | rs148158093 |
| PheGenI | rs148158093 |
| Biobank | rs148158093 |
| 1000 genomes | rs148158093 |
| hgdp | rs148158093 |
| ensembl | rs148158093 |
| geneview | rs148158093 |
| scholar | rs148158093 |
| rs148158093 | |
| pharmgkb | rs148158093 |
| gwascentral | rs148158093 |
| openSNP | rs148158093 |
| 23andMe | rs148158093 |
| SNPshot | rs148158093 |
| SNPdbe | rs148158093 |
| MSV3d | rs148158093 |
| GWAS Ctlg | rs148158093 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs148158093(A;A) |
| Alt | rs148158093(A;A) |
| Reference | Rs148158093(G;G) |
| Significance | Other |
| Disease | not specified Fabry disease |
| Variation | info |
| Gene | RPL36A-HNRNPH2 GLA |
| CLNDBN | not specified Fabry disease |
| Reversed | 0 |
| HGVS | NC_000023.10:g.100658816G>A |
| CLNSRC | HGMD |
| CLNACC | RCV000035303.6, RCV000078277.6, |
