rs553119528, GRN

N. diseases: 3
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.
Primary Progressive Nonfluent Aphasia
13 0.882 0.160 17 44352489 missense variant G/A snv 5.2E-05 6.3E-05 0.020 1.000 2 2009 2010
Dementia
CUI: C0497327
Disease: Dementia
176 0.882 0.160 17 44352489 missense variant G/A snv 5.2E-05 6.3E-05 0.010 1.000 1 2010 2010
Presenile dementia
CUI: C0011265
Disease: Presenile dementia
159 0.882 0.160 17 44352489 missense variant G/A snv 5.2E-05 6.3E-05 0.010 1.000 1 2010 2010