rs875989947
From SNPedia
					| Orientation | plus | 
| Stabilized | plus | 
| Geno | Mag | Summary | 
|---|---|---|
| (-;-) | 0 | common in clinvar | 
| Make rs875989947(-;CTGC) | 
| Make rs875989947(CTGC;CTGC) | 
| Reference | GRCh38.p2 38.2/147 | 
| Chromosome | 4 | 
| Position | 1001704 | 
| Gene | IDUA | 
| is a | snp | 
| is | mentioned by | 
| dbSNP | rs875989947 | 
| dbSNP (classic) | rs875989947 | 
| ClinGen | rs875989947 | 
| ebi | rs875989947 | 
| HLI | rs875989947 | 
| Exac | rs875989947 | 
| Gnomad | rs875989947 | 
| Varsome | rs875989947 | 
| LitVar | rs875989947 | 
| Map | rs875989947 | 
| PheGenI | rs875989947 | 
| Biobank | rs875989947 | 
| 1000 genomes | rs875989947 | 
| hgdp | rs875989947 | 
| ensembl | rs875989947 | 
| geneview | rs875989947 | 
| scholar | rs875989947 | 
| rs875989947 | |
| pharmgkb | rs875989947 | 
| gwascentral | rs875989947 | 
| openSNP | rs875989947 | 
| 23andMe | rs875989947 | 
| SNPshot | rs875989947 | 
| SNPdbe | rs875989947 | 
| MSV3d | rs875989947 | 
| GWAS Ctlg | rs875989947 | 
| Max Magnitude | 0 | 
| ClinVar | |
|---|---|
| Risk | rs875989947(TGCC;TGCC) | 
| Alt | rs875989947(TGCC;TGCC) | 
| Reference | Rs875989947(-;-) | 
| Significance | Pathogenic | 
| Disease | Hurler syndrome | 
| Variation | info | 
| Gene | IDUA | 
| CLNDBN | Hurler syndrome | 
| Reversed | 0 | 
| HGVS | NC_000004.11:g.995489_995492dupCTGC | 
| CLNSRC | Shahid Beheshti University of Medical Sciences | 
| CLNACC | RCV000211625.1, | 
