Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1060499939
rs1060499939
CUI: C0037772
Disease: Spastic Paraplegia
Spastic Paraplegia
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1060499939
rs1060499939
CUI: C0037772
Disease: Spastic Paraplegia
Spastic Paraplegia
T 0.700 GeneticVariation CLINVAR