rs1557043622, SLC35A2

N. diseases: 46
Disease: Hypoalbuminemia ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hypoalbuminemia
CUI: C0239981
Disease: Hypoalbuminemia
0.700 GeneticVariation CLINVAR SLC35A2-CDG: Functional characterization, expanded molecular, clinical, and biochemical phenotypes of 30 unreported Individuals. 30817854 2019