rs1557043622, SLC35A2

N. diseases: 46
Disease: Hypsarrhythmia ×
Source: CLINVAR ×
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hypsarrhythmia
CUI: C0684276
Disease: Hypsarrhythmia
0.700 GeneticVariation CLINVAR SLC35A2-CDG: Functional characterization, expanded molecular, clinical, and biochemical phenotypes of 30 unreported Individuals. 30817854 2019