rs1554107200, HARS1

N. diseases: 4
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2W
CUI: C4225265
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2W
0.700 GeneticVariation CLINVAR
Cerebellar atrophy
CUI: C0740279
Disease: Cerebellar atrophy
0.700 GeneticVariation CLINVAR
Impaired cognition
CUI: C0338656
Disease: Impaired cognition
0.700 GeneticVariation CLINVAR
Peripheral demyelinating neuropathy
CUI: C0270922
Disease: Peripheral demyelinating neuropathy
0.700 GeneticVariation CLINVAR