CRYAB, crystallin alpha B, 1410

N. diseases: 200; N. variants: 30
Disease: Myofibrillar Myopathy ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs281865141
rs281865141
Entrez Id: 1410;3316;100528019
Gene Symbol: CRYAB;HSPB2;HSPB2-C11orf52
CRYAB;HSPB2;HSPB2-C11orf52
CUI: C2678065
Disease:
Myofibrillar Myopathy 		T 0.700 CausalMutation CLINVAR