rs2454727, HCAR2

N. diseases: 3
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.
Atherothrombosis
CUI: C1963943
Disease: Atherothrombosis
15 0.925 0.040 12 122702333 missense variant C/T snv 0.010 1.000 1 2017 2017
Hypertriglyceridemia
CUI: C0020557
Disease: Hypertriglyceridemia
169 0.925 0.040 12 122702333 missense variant C/T snv 0.010 1.000 1 2017 2017
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.925 0.040 12 122702333 missense variant C/T snv 0.010 1.000 1 2017 2017