rs342293, CTB-30L5.1

N. diseases: 7
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.
Platelet mean volume determination (procedure)
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
371 0.882 0.040 7 106731773 intron variant C/G snv 0.42 0.800 1.000 7 2009 2019
Platelet Count measurement
CUI: C0032181
Disease: Platelet Count measurement
457 0.882 0.040 7 106731773 intron variant C/G snv 0.42 0.700 1.000 2 2012 2019
White Blood Cell Count procedure
CUI: C0023508
Disease: White Blood Cell Count procedure
1322 0.882 0.040 7 106731773 intron variant C/G snv 0.42 0.700 1.000 1 2019 2019
cardiac event
CUI: C0741923
Disease: cardiac event
18 0.882 0.040 7 106731773 intron variant C/G snv 0.42 0.010 1.000 1 2014 2014
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.882 0.040 7 106731773 intron variant C/G snv 0.42 0.010 1.000 1 2014 2014
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.882 0.040 7 106731773 intron variant C/G snv 0.42 0.010 1.000 1 2014 2014
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.882 0.040 7 106731773 intron variant C/G snv 0.42 0.010 1.000 1 2014 2014