rs1560618505, ZEB2

N. diseases: 1
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Mowat-Wilson syndrome
CUI: C1856113
Disease: Mowat-Wilson syndrome
0.700 CausalMutation CLINVAR ZFHX1B mutations in patients with Mowat-Wilson syndrome. 17203459 2007