rs12041331, PEAR1

N. diseases: 11
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 Component Distribution Width Measurement
CUI: C3828530
Disease: Platelet Component Distribution Width Measurement
200 0.776 0.200 1 156899922 intron variant G/A snv 0.19 0.700 1.000 1 2016 2016
Platelet Count measurement
CUI: C0032181
Disease: Platelet Count measurement
457 0.776 0.200 1 156899922 intron variant G/A snv 0.19 0.700 1.000 1 2018 2018
Platelet mean volume determination (procedure)
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
371 0.776 0.200 1 156899922 intron variant G/A snv 0.19 0.700 1.000 1 2016 2016
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.776 0.200 1 156899922 intron variant G/A snv 0.19 0.020 1.000 2 2014 2017
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.776 0.200 1 156899922 intron variant G/A snv 0.19 0.020 1.000 2 2014 2017
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.776 0.200 1 156899922 intron variant G/A snv 0.19 0.020 1.000 2 2014 2017
AURAL ATRESIA, CONGENITAL
CUI: C1842937
Disease: AURAL ATRESIA, CONGENITAL
29 0.776 0.200 1 156899922 intron variant G/A snv 0.19 0.010 1.000 1 2019 2019
Coronary Aneurysm
CUI: C0010051
Disease: Coronary Aneurysm
17 0.776 0.200 1 156899922 intron variant G/A snv 0.19 0.010 1.000 1 2019 2019
Mucocutaneous Lymph Node Syndrome
CUI: C0026691
Disease: Mucocutaneous Lymph Node Syndrome
195 0.776 0.200 1 156899922 intron variant G/A snv 0.19 0.010 1.000 1 2019 2019
Multiple Chronic Conditions
CUI: C3266262
Disease: Multiple Chronic Conditions
42 0.776 0.200 1 156899922 intron variant G/A snv 0.19 0.010 1.000 1 2013 2013
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.776 0.200 1 156899922 intron variant G/A snv 0.19 0.010 1.000 1 2013 2013