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: rs80358229
rs80358229
Entrez Id: 81031
Gene Symbol: SLC2A10
SLC2A10
CUI: C1859726
Disease:
ARTERIAL TORTUOSITY SYNDROME 		A 0.700 CausalMutation CLINVAR Arterial tortuosity syndrome: early diagnosis and association with venous tortuosity. 23410549 2013
dbSNP: rs80358229
rs80358229
Entrez Id: 81031
Gene Symbol: SLC2A10
SLC2A10
CUI: C1859726
Disease:
ARTERIAL TORTUOSITY SYNDROME 		A 0.700 CausalMutation CLINVAR Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome. 16550171 2006