rs371282890, LPL

N. diseases: 6
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 I
CUI: C0023817
Disease: Hyperlipoproteinemia Type I
64 0.827 0.120 8 19955900 missense variant C/G snv 1.1E-04 6.3E-05 0.720 1.000 22 1990 2016
Hypertriglyceridemia
CUI: C0020557
Disease: Hypertriglyceridemia
169 0.827 0.120 8 19955900 missense variant C/G snv 1.1E-04 6.3E-05 0.030 1.000 3 2000 2016
Acute pancreatitis
CUI: C0001339
Disease: Acute pancreatitis
51 0.827 0.120 8 19955900 missense variant C/G snv 1.1E-04 6.3E-05 0.010 1.000 1 2014 2014
Familial hyperchylomicronemia syndrome
CUI: C2931862
Disease: Familial hyperchylomicronemia syndrome
2 0.827 0.120 8 19955900 missense variant C/G snv 1.1E-04 6.3E-05 0.010 1.000 1 2006 2006
Pancreatitis, Chronic
CUI: C0149521
Disease: Pancreatitis, Chronic
56 0.827 0.120 8 19955900 missense variant C/G snv 1.1E-04 6.3E-05 0.010 1.000 1 2016 2016
Recurrent pancreatitis
CUI: C4551632
Disease: Recurrent pancreatitis
13 0.827 0.120 8 19955900 missense variant C/G snv 1.1E-04 6.3E-05 0.010 1.000 1 2016 2016