rs587784568
From SNPedia
					| Orientation | minus | 
| Stabilized | minus | 
| Geno | Mag | Summary | 
|---|---|---|
| (TCTCGCCTTGGCACGCCAG;TCTCGCCTTGGCACGCCAG) | 0 | common in clinvar | 
| Make rs587784568(-;-) | 
| Make rs587784568(-;TCTCGCCTTGGCACGCCAG) | 
| Reference | GRCh38.p2 38.2/144 | 
| Chromosome | 2 | 
| Position | 144404860 | 
| Gene | ZEB2 | 
| is a | snp | 
| is | mentioned by | 
| dbSNP | rs587784568 | 
| dbSNP (classic) | rs587784568 | 
| ClinGen | rs587784568 | 
| ebi | rs587784568 | 
| HLI | rs587784568 | 
| Exac | rs587784568 | 
| Gnomad | rs587784568 | 
| Varsome | rs587784568 | 
| LitVar | rs587784568 | 
| Map | rs587784568 | 
| PheGenI | rs587784568 | 
| Biobank | rs587784568 | 
| 1000 genomes | rs587784568 | 
| hgdp | rs587784568 | 
| ensembl | rs587784568 | 
| geneview | rs587784568 | 
| scholar | rs587784568 | 
| rs587784568 | |
| pharmgkb | rs587784568 | 
| gwascentral | rs587784568 | 
| openSNP | rs587784568 | 
| 23andMe | rs587784568 | 
| SNPshot | rs587784568 | 
| SNPdbe | rs587784568 | 
| MSV3d | rs587784568 | 
| GWAS Ctlg | rs587784568 | 
| Max Magnitude | 0 | 
| ClinVar | |
|---|---|
| Risk | rs587784568(-;-) | 
| Alt | rs587784568(-;-) | 
| Reference | Rs587784568(TCTCGCCTTGGCACGCCAG;TCTCGCCTTGGCACGCCAG) | 
| Significance | Pathogenic | 
| Disease | Mowat-Wilson syndrome | 
| Variation | info | 
| Gene | ZEB2 | 
| CLNDBN | Mowat-Wilson syndrome | 
| Reversed | 1 | 
| HGVS | NC_000002.11:g.145162427_145162445del19 | 
| CLNSRC | |
| CLNACC | RCV000148003.1, | 


