rs669, A2M;KLRG1

N. diseases: 7
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 DISEASE, SUSCEPTIBILITY TO
CUI: C1856170
Disease: ALZHEIMER DISEASE, SUSCEPTIBILITY TO
3 0.851 0.080 12 9079672 missense variant T/C snv 0.31 0.33 0.700 0
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.851 0.080 12 9079672 missense variant T/C snv 0.31 0.33 0.070 0.714 7 1999 2014
Abnormal behavior
CUI: C0233514
Disease: Abnormal behavior
121 0.851 0.080 12 9079672 missense variant T/C snv 0.31 0.33 0.010 1.000 1 2000 2000
Argyrophilic grain disease
CUI: C0338460
Disease: Argyrophilic grain disease
7 0.851 0.080 12 9079672 missense variant T/C snv 0.31 0.33 0.010 1.000 1 2002 2002
Mental disorders
CUI: C0004936
Disease: Mental disorders
149 0.851 0.080 12 9079672 missense variant T/C snv 0.31 0.33 0.010 1.000 1 2000 2000
Mild cognitive disorder
CUI: C1270972
Disease: Mild cognitive disorder
96 0.851 0.080 12 9079672 missense variant T/C snv 0.31 0.33 0.010 1.000 1 2000 2000
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.851 0.080 12 9079672 missense variant T/C snv 0.31 0.33 0.010 1.000 1 2016 2016