SCARB2, scavenger receptor class B member 2, 950

N. diseases: 103; N. variants: 28
Disease: Action Myoclonus-Renal Failure Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs755903502
rs755903502
Entrez Id: 950
Gene Symbol: SCARB2
SCARB2
CUI: C0751779
Disease:
Action Myoclonus-Renal Failure Syndrome 		C 0.700 CausalMutation CLINVAR A mutation in SCARB2 is a modifier in Gaucher disease. 21796727 2011