rs755042147
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs755042147(-;-) |
| Make rs755042147(-;T) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 19 |
| Position | 7528639 |
| Gene | MCOLN1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs755042147 |
| dbSNP (classic) | rs755042147 |
| ClinGen | rs755042147 |
| ebi | rs755042147 |
| HLI | rs755042147 |
| Exac | rs755042147 |
| Gnomad | rs755042147 |
| Varsome | rs755042147 |
| LitVar | rs755042147 |
| Map | rs755042147 |
| PheGenI | rs755042147 |
| Biobank | rs755042147 |
| 1000 genomes | rs755042147 |
| hgdp | rs755042147 |
| ensembl | rs755042147 |
| geneview | rs755042147 |
| scholar | rs755042147 |
| rs755042147 | |
| pharmgkb | rs755042147 |
| gwascentral | rs755042147 |
| openSNP | rs755042147 |
| 23andMe | rs755042147 |
| SNPshot | rs755042147 |
| SNPdbe | rs755042147 |
| MSV3d | rs755042147 |
| GWAS Ctlg | rs755042147 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs755042147(-;-) |
| Alt | rs755042147(-;-) |
| Reference | Rs755042147(T;T) |
| Significance | Other |
| Disease | Ganglioside sialidase deficiency |
| Variation | info |
| Gene | MCOLN1 |
| CLNDBN | Ganglioside sialidase deficiency |
| Reversed | 0 |
| HGVS | NC_000019.9:g.7593525delT |
| CLNSRC | |
| CLNACC | RCV000194725.1, |
