rs148789453
From SNPedia
					| Orientation | plus | 
| Stabilized | plus | 
| Geno | Mag | Summary | 
|---|---|---|
| (T;T) | 0 | common in clinvar | 
| Make rs148789453(A;A) | 
| Make rs148789453(A;T) | 
| Reference | GRCh38.p7 38.3/149 | 
| Chromosome | 4 | 
| Position | 1001802 | 
| Gene | IDUA | 
| is a | snp | 
| is | mentioned by | 
| dbSNP | rs148789453 | 
| dbSNP (classic) | rs148789453 | 
| ClinGen | rs148789453 | 
| ebi | rs148789453 | 
| HLI | rs148789453 | 
| Exac | rs148789453 | 
| Gnomad | rs148789453 | 
| Varsome | rs148789453 | 
| LitVar | rs148789453 | 
| Map | rs148789453 | 
| PheGenI | rs148789453 | 
| Biobank | rs148789453 | 
| 1000 genomes | rs148789453 | 
| hgdp | rs148789453 | 
| ensembl | rs148789453 | 
| geneview | rs148789453 | 
| scholar | rs148789453 | 
| rs148789453 | |
| pharmgkb | rs148789453 | 
| gwascentral | rs148789453 | 
| openSNP | rs148789453 | 
| 23andMe | rs148789453 | 
| SNPshot | rs148789453 | 
| SNPdbe | rs148789453 | 
| MSV3d | rs148789453 | 
| GWAS Ctlg | rs148789453 | 
| Max Magnitude | 0 | 
| ClinVar | |
|---|---|
| Risk | rs148789453(A;A) rs148789453(G;G) | 
| Alt | rs148789453(A;A) rs148789453(G;G) | 
| Reference | Rs148789453(T;T) | 
| Significance | Pathogenic | 
| Disease | not provided | 
| Variation | info | 
| Gene | IDUA | 
| CLNDBN | not provided | 
| Reversed | 0 | 
| HGVS | NC_000004.11:g.995590T>A | 
| CLNSRC | |
| CLNACC | RCV000256027.2, | 
