rs727503784
From SNPedia
					| Orientation | minus | 
| Stabilized | minus | 
| Geno | Mag | Summary | 
|---|---|---|
| (T;T) | 0 | common in clinvar | 
| Make rs727503784(-;-) | 
| Make rs727503784(-;T) | 
| Reference | GRCh38.p2 38.2/144 | 
| Chromosome | 2 | 
| Position | 144429811 | 
| Gene | ZEB2 | 
| is a | snp | 
| is | mentioned by | 
| dbSNP | rs727503784 | 
| dbSNP (classic) | rs727503784 | 
| ClinGen | rs727503784 | 
| ebi | rs727503784 | 
| HLI | rs727503784 | 
| Exac | rs727503784 | 
| Gnomad | rs727503784 | 
| Varsome | rs727503784 | 
| LitVar | rs727503784 | 
| Map | rs727503784 | 
| PheGenI | rs727503784 | 
| Biobank | rs727503784 | 
| 1000 genomes | rs727503784 | 
| hgdp | rs727503784 | 
| ensembl | rs727503784 | 
| geneview | rs727503784 | 
| scholar | rs727503784 | 
| rs727503784 | |
| pharmgkb | rs727503784 | 
| gwascentral | rs727503784 | 
| openSNP | rs727503784 | 
| 23andMe | rs727503784 | 
| SNPshot | rs727503784 | 
| SNPdbe | rs727503784 | 
| MSV3d | rs727503784 | 
| GWAS Ctlg | rs727503784 | 
| Max Magnitude | 0 | 
| ClinVar | |
|---|---|
| Risk | rs727503784(-;-) | 
| Alt | rs727503784(-;-) | 
| Reference | Rs727503784(T;T) | 
| Significance | Pathogenic | 
| Disease | Mowat-Wilson syndrome | 
| Variation | info | 
| Gene | ZEB2 | 
| CLNDBN | Mowat-Wilson syndrome | 
| Reversed | 1 | 
| HGVS | NC_000002.11:g.145187378delA | 
| CLNSRC | |
| CLNACC | RCV000157060.3, | 


