Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894351
rs104894351
Entrez Id: 26353;107984440
Gene Symbol: HSPB8;LOC107984440
HSPB8;LOC107984440
CUI: C0235025
Disease:
Peripheral motor neuropathy
0.010 GeneticVariation BEFREE Some properties of the K141E mutant of human HSP22 that is expressed in distal hereditary motor neuropathy were investigated. 16949546 2006