rs886039227, DCTN1

N. diseases: 4
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Perry Syndrome
CUI: C1868594
Disease: Perry Syndrome
9 0.925 0.200 2 74378123 missense variant A/C snv 0.820 1.000 8 2009 2018
Parkinsonian Disorders
CUI: C0242422
Disease: Parkinsonian Disorders
95 0.925 0.200 2 74378123 missense variant A/C snv 0.020 1.000 2 2014 2018
Progressive supranuclear palsy
CUI: C0038868
Disease: Progressive supranuclear palsy
52 0.925 0.200 2 74378123 missense variant A/C snv 0.010 1.000 1 2018 2018
Tauopathies
CUI: C0949664
Disease: Tauopathies
43 0.925 0.200 2 74378123 missense variant A/C snv 0.010 1.000 1 2018 2018