rs1386984902, APP

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 0.160 21 26000095 missense variant G/A snv 0.100 1.000 12 2003 2020
Central neuroblastoma
CUI: C0700095
Disease: Central neuroblastoma
231 0.790 0.160 21 26000095 missense variant G/A snv 0.040 1.000 4 2006 2020
Childhood Neuroblastoma
CUI: C4086165
Disease: Childhood Neuroblastoma
231 0.790 0.160 21 26000095 missense variant G/A snv 0.040 1.000 4 2006 2020
Neuroblastoma
CUI: C0027819
Disease: Neuroblastoma
386 0.790 0.160 21 26000095 missense variant G/A snv 0.040 1.000 4 2006 2020
Tauopathies
CUI: C0949664
Disease: Tauopathies
43 0.790 0.160 21 26000095 missense variant G/A snv 0.040 1.000 4 2006 2020
Cognition Disorders
CUI: C0009241
Disease: Cognition Disorders
47 0.790 0.160 21 26000095 missense variant G/A snv 0.010 1.000 1 2016 2016
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
215 0.790 0.160 21 26000095 missense variant G/A snv 0.010 1.000 1 2016 2016
Impaired cognition
CUI: C0338656
Disease: Impaired cognition
348 0.790 0.160 21 26000095 missense variant G/A snv 0.010 1.000 1 2016 2016
Pick Disease of the Brain
CUI: C0236642
Disease: Pick Disease of the Brain
83 0.790 0.160 21 26000095 missense variant G/A snv 0.010 1.000 1 2016 2016