rs587778556, NFE2L2

N. diseases: 2
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.
Tauopathies
CUI: C0949664
Disease: Tauopathies
43 2 177231705 missense variant G/A snv 3.2E-05 4.9E-05 0.020 1.000 2 2014 2018
Neurodegenerative Disorders
CUI: C0524851
Disease: Neurodegenerative Disorders
85 2 177231705 missense variant G/A snv 3.2E-05 4.9E-05 0.010 1.000 1 2014 2014