rs12566888, PEAR1

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 aggregation
CUI: C0032176
Disease: Platelet aggregation
11 0.807 0.280 1 156899255 intron variant G/T snv 0.26 0.700 1.000 1 2010 2010
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.807 0.280 1 156899255 intron variant G/T snv 0.26 0.010 1.000 1 2018 2018
Acute Coronary Syndrome
CUI: C0948089
Disease: Acute Coronary Syndrome
139 0.807 0.280 1 156899255 intron variant G/T snv 0.26 0.010 1.000 1 2018 2018
AURAL ATRESIA, CONGENITAL
CUI: C1842937
Disease: AURAL ATRESIA, CONGENITAL
29 0.807 0.280 1 156899255 intron variant G/T snv 0.26 0.010 1.000 1 2019 2019
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.807 0.280 1 156899255 intron variant G/T snv 0.26 0.010 1.000 1 2018 2018
SMALL PATELLA SYNDROME
CUI: C1840061
Disease: SMALL PATELLA SYNDROME
15 0.807 0.280 1 156899255 intron variant G/T snv 0.26 0.010 1.000 1 2015 2015
Stiff-Person Syndrome
CUI: C0085292
Disease: Stiff-Person Syndrome
9 0.807 0.280 1 156899255 intron variant G/T snv 0.26 0.010 1.000 1 2015 2015