rs9551963, ALOX5AP

N. diseases: 6
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.
Cerebral Infarction
CUI: C0007785
Disease: Cerebral Infarction
123 0.851 0.160 13 30758410 intron variant A/C;T snv 0.020 1.000 2 2012 2014
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.851 0.160 13 30758410 intron variant A/C;T snv 0.020 1.000 2 2014 2015
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.851 0.160 13 30758410 intron variant A/C;T snv 0.020 0.500 2 2012 2019
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.851 0.160 13 30758410 intron variant A/C;T snv 0.010 1.000 1 2012 2012
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.851 0.160 13 30758410 intron variant A/C;T snv 0.010 1.000 1 2016 2016
Xanthoma
CUI: C0302314
Disease: Xanthoma
4 0.851 0.160 13 30758410 intron variant A/C;T snv 0.010 1.000 1 2009 2009