rs3764650, ABCA7

N. diseases: 9
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.
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.790 0.200 19 1046521 intron variant T/G snv 0.14 0.900 1.000 11 2011 2019
Prion Diseases
CUI: C0162534
Disease: Prion Diseases
67 0.790 0.200 19 1046521 intron variant T/G snv 0.14 0.700 1.000 1 2012 2012
Alzheimer Disease, Late Onset
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
243 0.790 0.200 19 1046521 intron variant T/G snv 0.14 0.030 1.000 3 2015 2020
Dementia
CUI: C0497327
Disease: Dementia
176 0.790 0.200 19 1046521 intron variant T/G snv 0.14 0.010 1.000 1 2019 2019
Familial lichen amyloidosis
CUI: C0268398
Disease: Familial lichen amyloidosis
24 0.790 0.200 19 1046521 intron variant T/G snv 0.14 0.010 1.000 1 2014 2014
Impaired cognition
CUI: C0338656
Disease: Impaired cognition
348 0.790 0.200 19 1046521 intron variant T/G snv 0.14 0.010 1.000 1 2019 2019
Mental deterioration
CUI: C0234985
Disease: Mental deterioration
121 0.790 0.200 19 1046521 intron variant T/G snv 0.14 0.010 1.000 1 2019 2019
Mild cognitive disorder
CUI: C1270972
Disease: Mild cognitive disorder
96 0.790 0.200 19 1046521 intron variant T/G snv 0.14 0.010 1.000 1 2015 2015
Presenile dementia
CUI: C0011265
Disease: Presenile dementia
159 0.790 0.200 19 1046521 intron variant T/G snv 0.14 0.010 1.000 1 2019 2019