rs1131882, TBXA2R

N. diseases: 3
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.
Asthma
CUI: C0004096
Disease: Asthma
1536 0.882 0.200 19 3595925 missense variant G/A snv 0.22 0.15 0.020 1.000 2 2007 2013
Carotid Stenosis
CUI: C0007282
Disease: Carotid Stenosis
19 0.882 0.200 19 3595925 missense variant G/A snv 0.22 0.15 0.010 1.000 1 2019 2019
Cerebral Infarction
CUI: C0007785
Disease: Cerebral Infarction
123 0.882 0.200 19 3595925 missense variant G/A snv 0.22 0.15 0.010 1.000 1 2015 2015