TBXA2R, thromboxane A2 receptor, 6915

N. diseases: 83; N. variants: 11
Disease: Cerebral Infarction ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs4523
rs4523 		0.776 0.280 19 3595796 missense variant A/G snv 0.56 0.66
CUI: C0007785
Disease: Cerebral Infarction
Cerebral Infarction 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases 0.020 1.000 2 2013 2015
dbSNP: rs1131882
rs1131882 		0.882 0.200 19 3595925 missense variant G/A snv 0.22 0.15
CUI: C0007785
Disease: Cerebral Infarction
Cerebral Infarction 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs2238634
rs2238634 		0.925 0.200 19 3604731 intron variant A/C;T snv
CUI: C0007785
Disease: Cerebral Infarction
Cerebral Infarction 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2006 2006