rs9943291, HMGCS2

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.
elevated blood glucose level
CUI: C0495706
Disease: elevated blood glucose level
111 1 119749667 intron variant T/G snv 8.2E-02 0.700 1.000 1 2018 2018
Glucose measurement
CUI: C0337438
Disease: Glucose measurement
111 1 119749667 intron variant T/G snv 8.2E-02 0.700 1.000 1 2018 2018
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 1 119749667 intron variant T/G snv 8.2E-02 0.700 1.000 1 2018 2018