rs878853324, PPT1

N. diseases: 5
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Cerebellar cortical atrophy
CUI: C4024710
Disease: Cerebellar cortical atrophy
0.700 GeneticVariation CLINVAR
CEROID LIPOFUSCINOSIS, NEURONAL, 1
CUI: C1850451
Disease: CEROID LIPOFUSCINOSIS, NEURONAL, 1
0.700 GeneticVariation CLINVAR
Cerebral atrophy
CUI: C0235946
Disease: Cerebral atrophy
0.700 GeneticVariation CLINVAR
Reduced visual acuity
CUI: C0234632
Disease: Reduced visual acuity
0.700 GeneticVariation CLINVAR
Seizures
CUI: C0036572
Disease: Seizures
0.700 GeneticVariation CLINVAR