rs587779401
From SNPedia
					| Orientation | plus | 
| Stabilized | plus | 
| Geno | Mag | Summary | 
|---|---|---|
| (A;A) | 0 | common in clinvar | 
| Make rs587779401(A;G) | 
| Make rs587779401(G;G) | 
| Reference | GRCh38.p2 38.2/144 | 
| Chromosome | 4 | 
| Position | 1004305 | 
| Gene | IDUA | 
| is a | snp | 
| is | mentioned by | 
| dbSNP | rs587779401 | 
| dbSNP (classic) | rs587779401 | 
| ClinGen | rs587779401 | 
| ebi | rs587779401 | 
| HLI | rs587779401 | 
| Exac | rs587779401 | 
| Gnomad | rs587779401 | 
| Varsome | rs587779401 | 
| LitVar | rs587779401 | 
| Map | rs587779401 | 
| PheGenI | rs587779401 | 
| Biobank | rs587779401 | 
| 1000 genomes | rs587779401 | 
| hgdp | rs587779401 | 
| ensembl | rs587779401 | 
| geneview | rs587779401 | 
| scholar | rs587779401 | 
| rs587779401 | |
| pharmgkb | rs587779401 | 
| gwascentral | rs587779401 | 
| openSNP | rs587779401 | 
| 23andMe | rs587779401 | 
| SNPshot | rs587779401 | 
| SNPdbe | rs587779401 | 
| MSV3d | rs587779401 | 
| GWAS Ctlg | rs587779401 | 
| Max Magnitude | 0 | 
| ClinVar | |
|---|---|
| Risk | rs587779401(G;G) | 
| Alt | rs587779401(G;G) | 
| Reference | Rs587779401(A;A) | 
| Significance | Pathogenic | 
| Disease | Hurler syndrome | 
| Variation | info | 
| Gene | IDUA | 
| CLNDBN | Hurler syndrome | 
| Reversed | 0 | 
| HGVS | NC_000004.11:g.998093A>G | 
| CLNSRC | |
| CLNACC | RCV000087088.1, | 
