rs1799822, CPT2

N. diseases: 4
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.
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 0.925 0.080 1 53213557 missense variant A/G snv 0.16 0.15 0.010 1.000 1 1992 1992
Encephalitis
CUI: C0014038
Disease: Encephalitis
18 0.925 0.080 1 53213557 missense variant A/G snv 0.16 0.15 0.010 1.000 1 2019 2019
Enterovirus Infections
CUI: C0014378
Disease: Enterovirus Infections
12 0.925 0.080 1 53213557 missense variant A/G snv 0.16 0.15 0.010 1.000 1 2019 2019
Hypoglycemia
CUI: C0020615
Disease: Hypoglycemia
42 0.925 0.080 1 53213557 missense variant A/G snv 0.16 0.15 0.010 1.000 1 1992 1992