Gene: SPG11 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs312262717
rs312262717
SPG11
C 0.700 CausalMutation CLINVAR SPG11 mutations cause Kjellin syndrome, a hereditary spastic paraplegia with thin corpus callosum and central retinal degeneration. 19194956

2009
dbSNP: rs1057518874
rs1057518874
SPG11
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1555454508
rs1555454508
SPG11
ATC 0.700 CausalMutation CLINVAR

dbSNP: rs201689565
rs201689565
SPG11
G 0.700 GeneticVariation CLINVAR