rs10507391, ALOX5AP

N. diseases: 10
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.
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.776 0.320 13 30737959 intron variant A/T snv 0.52 0.040 1.000 4 2011 2016
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.776 0.320 13 30737959 intron variant A/T snv 0.52 0.030 0.667 3 2015 2019
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.776 0.320 13 30737959 intron variant A/T snv 0.52 0.010 1 2014 2014
Acute Coronary Syndrome
CUI: C0948089
Disease: Acute Coronary Syndrome
139 0.776 0.320 13 30737959 intron variant A/T snv 0.52 0.010 1.000 1 2014 2014
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.776 0.320 13 30737959 intron variant A/T snv 0.52 0.010 1.000 1 2016 2016
Asthma
CUI: C0004096
Disease: Asthma
1536 0.776 0.320 13 30737959 intron variant A/T snv 0.52 0.010 1.000 1 2010 2010
Cerebral Infarction
CUI: C0007785
Disease: Cerebral Infarction
123 0.776 0.320 13 30737959 intron variant A/T snv 0.52 0.010 1 2015 2015
Lung Diseases, Interstitial
CUI: C0206062
Disease: Lung Diseases, Interstitial
144 0.776 0.320 13 30737959 intron variant A/T snv 0.52 0.010 1.000 1 2017 2017
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.776 0.320 13 30737959 intron variant A/T snv 0.52 0.010 1.000 1 2019 2019
Ventilatory defect
CUI: C0231926
Disease: Ventilatory defect
1 0.776 0.320 13 30737959 intron variant A/T snv 0.52 0.010 1.000 1 2017 2017