rs1557196978, ATP6AP1

N. diseases: 8
Disease: Hepatosplenomegaly ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hepatosplenomegaly
CUI: C0019214
Disease: Hepatosplenomegaly
0.700 CausalMutation CLINVAR Cutis laxa, exocrine pancreatic insufficiency and altered cellular metabolomics as additional symptoms in a new patient with ATP6AP1-CDG. 29396028 2018