VPS13B, vacuolar protein sorting 13 homolog B, 157680

N. diseases: 158; N. variants: 309
Disease: Retinal Dystrophies ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057518939
rs1057518939
Entrez Id: 157680
Gene Symbol: VPS13B
VPS13B
CUI: C0854723
Disease:
Retinal Dystrophies 		C 0.700 CausalMutation CLINVAR
dbSNP: rs386834061
rs386834061
Entrez Id: 157680
Gene Symbol: VPS13B
VPS13B
CUI: C0854723
Disease:
Retinal Dystrophies 		T 0.700 CausalMutation CLINVAR