rs573658040, APOE

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.
Hyperlipoproteinemia Type III
CUI: C0020479
Disease: Hyperlipoproteinemia Type III
24 0.790 0.200 19 44908705 missense variant C/G;T snv 6.3E-06 0.100 0.900 10 1991 2014
Hyperkeratosis lenticularis perstans
CUI: C0263420
Disease: Hyperkeratosis lenticularis perstans
11 0.790 0.200 19 44908705 missense variant C/G;T snv 6.3E-06 0.020 1.000 2 1996 2006
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
184 0.790 0.200 19 44908705 missense variant C/G;T snv 6.3E-06 0.010 1.000 1 2014 2014
Hypercholesterolemia
CUI: C0020443
Disease: Hypercholesterolemia
123 0.790 0.200 19 44908705 missense variant C/G;T snv 6.3E-06 0.010 1.000 1 2000 2000
Hyperlipidemia
CUI: C0020473
Disease: Hyperlipidemia
83 0.790 0.200 19 44908705 missense variant C/G;T snv 6.3E-06 0.010 1.000 1 1995 1995
Hyperlipoproteinemias
CUI: C0020476
Disease: Hyperlipoproteinemias
7 0.790 0.200 19 44908705 missense variant C/G;T snv 6.3E-06 0.010 1.000 1 2000 2000
Hypertriglyceridemia
CUI: C0020557
Disease: Hypertriglyceridemia
169 0.790 0.200 19 44908705 missense variant C/G;T snv 6.3E-06 0.010 1.000 1 1998 1998
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.790 0.200 19 44908705 missense variant C/G;T snv 6.3E-06 0.010 1.000 1 2009 2009
Tuberous xanthoma
CUI: C0302164
Disease: Tuberous xanthoma
2 0.790 0.200 19 44908705 missense variant C/G;T snv 6.3E-06 0.010 1.000 1 2006 2006