Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs118203986
rs118203986
0.010 GeneticVariation BEFREE Of particular health-related interest is the mutation Histidine 147 to Arginine (H147R) in human TRiC subunit 5 (CCT5), which has been associated with hereditary sensory neuropathy. 28623285

2017

dbSNP: rs775437084
rs775437084
0.010 GeneticVariation BEFREE The Variant p.(Arg183Trp) in SPTLC2 Causes Late-Onset Hereditary Sensory Neuropathy. 26573920

2016