Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs587778556
rs587778556
NFE2L2
2 177231705 missense variant G/A snv 3.2E-05 4.9E-05
CUI: C0949664
Disease: Tauopathies
Tauopathies 		0.020 1.000 2 2014 2018
dbSNP: rs587778556
rs587778556
NFE2L2
2 177231705 missense variant G/A snv 3.2E-05 4.9E-05
CUI: C0524851
Disease: Neurodegenerative Disorders
Neurodegenerative Disorders 		0.010 1.000 1 2014 2014