rs1553785033, SLC2A2

N. diseases: 6
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Global developmental delay
CUI: C0557874
Disease: Global developmental delay
0.700 GeneticVariation CLINVAR
Fanconi-Bickel Syndrome
CUI: C3495427
Disease: Fanconi-Bickel Syndrome
0.700 GeneticVariation CLINVAR
Chronic acidosis
CUI: C1735903
Disease: Chronic acidosis
0.700 GeneticVariation CLINVAR
Renal tubular disorder
CUI: C0151747
Disease: Renal tubular disorder
0.700 GeneticVariation CLINVAR
Impairment of galactose metabolism
CUI: C4021643
Disease: Impairment of galactose metabolism
0.700 GeneticVariation CLINVAR
Abdomen distended
CUI: C0000731
Disease: Abdomen distended
0.700 GeneticVariation CLINVAR