rs12632110, SEMA3F

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.
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 1.000 0.080 3 50186792 intron variant A/G snv 0.63 0.62 0.030 1.000 3 2009 2010
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 1.000 0.080 3 50186792 intron variant A/G snv 0.63 0.62 0.010 1.000 1 2009 2009
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 1.000 0.080 3 50186792 intron variant A/G snv 0.63 0.62 0.010 1.000 1 2009 2009