Difference between revisions of "Rs104894639"
From SNPedia
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Revision as of 23:38, 20 February 2012
| Orientation | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;G) | 3 | Carrier of a Sanfilippo syndrome type A mutation |
| (G;G) | 0 | common in clinvar |
| Make rs104894639(A;A) |
| Reference | GRCh37 37.1/132 |
| Chromosome | 17 |
| Position | 78184421 |
| Gene | SGSH |
| is a | snp |
| is | mentioned by |
| dbSNP | rs104894639 |
| dbSNP (classic) | rs104894639 |
| ClinGen | rs104894639 |
| ebi | rs104894639 |
| HLI | rs104894639 |
| Exac | rs104894639 |
| Gnomad | rs104894639 |
| Varsome | rs104894639 |
| LitVar | rs104894639 |
| Map | rs104894639 |
| PheGenI | rs104894639 |
| Biobank | rs104894639 |
| 1000 genomes | rs104894639 |
| hgdp | rs104894639 |
| ensembl | rs104894639 |
| geneview | rs104894639 |
| scholar | rs104894639 |
| rs104894639 | |
| pharmgkb | rs104894639 |
| gwascentral | rs104894639 |
| openSNP | rs104894639 |
| 23andMe | rs104894639 |
| SNPshot | rs104894639 |
| SNPdbe | rs104894639 |
| MSV3d | rs104894639 |
| GWAS Ctlg | rs104894639 |
| Max Magnitude | 3 |
