rs137852895
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Make rs137852895(A;G) |
| Make rs137852895(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 101770085 |
| Gene | GNPTAB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs137852895 |
| dbSNP (classic) | rs137852895 |
| ClinGen | rs137852895 |
| ebi | rs137852895 |
| HLI | rs137852895 |
| Exac | rs137852895 |
| Gnomad | rs137852895 |
| Varsome | rs137852895 |
| LitVar | rs137852895 |
| Map | rs137852895 |
| PheGenI | rs137852895 |
| Biobank | rs137852895 |
| 1000 genomes | rs137852895 |
| hgdp | rs137852895 |
| ensembl | rs137852895 |
| geneview | rs137852895 |
| scholar | rs137852895 |
| rs137852895 | |
| pharmgkb | rs137852895 |
| gwascentral | rs137852895 |
| openSNP | rs137852895 |
| 23andMe | rs137852895 |
| SNPshot | rs137852895 |
| SNPdbe | rs137852895 |
| MSV3d | rs137852895 |
| GWAS Ctlg | rs137852895 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs137852895(C;C) rs137852895(G;G) |
| Alt | rs137852895(C;C) rs137852895(G;G) |
| Reference | Rs137852895(A;A) |
| Significance | Pathogenic |
| Disease | Pseudo-Hurler polydystrophy |
| Variation | info |
| Gene | GNPTAB |
| CLNDBN | Pseudo-Hurler polydystrophy |
| Reversed | 1 |
| HGVS | NC_000012.11:g.102163863T>G |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000002889.4, |
[PMID 16094673] Missense mutations in N-acetylglucosamine-1-phosphotransferase alpha/beta subunit gene in a patient with mucolipidosis III and a mild clinical phenotype.
