rs781934508, SURF1

N. diseases: 4
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Dysarthria
CUI: C0013362
Disease: Dysarthria
0.700 GeneticVariation CLINVAR
Cerebellar Ataxia
CUI: C0007758
Disease: Cerebellar Ataxia
0.700 GeneticVariation CLINVAR
Pyramidal sign
CUI: C0234132
Disease: Pyramidal sign
0.700 GeneticVariation CLINVAR
Muscle Weakness
CUI: C0151786
Disease: Muscle Weakness
0.700 GeneticVariation CLINVAR