SLC2A10, solute carrier family 2 member 10, 81031

N. diseases: 135; N. variants: 22
Disease: ARTERIAL TORTUOSITY SYNDROME ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs146579504
rs146579504
Entrez Id: 81031
Gene Symbol: SLC2A10
SLC2A10
CUI: C1859726
Disease:
ARTERIAL TORTUOSITY SYNDROME 		T 0.700 CausalMutation CLINVAR Arterial tortuosity syndrome in two Italian paediatric patients. 19781076 2009
dbSNP: rs146579504
rs146579504
Entrez Id: 81031
Gene Symbol: SLC2A10
SLC2A10
CUI: C1859726
Disease:
ARTERIAL TORTUOSITY SYNDROME 		T 0.700 GeneticVariation CLINVAR