LTA, lymphotoxin alpha, 4049

N. diseases: 353; N. variants: 26
Disease: Myocardial 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: rs1041981
rs1041981 		0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.720 1.000 2 2005 2007
dbSNP: rs909253
rs909253 		0.641 0.600 6 31572536 intron variant A/G;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 0
dbSNP: rs1800683
rs1800683 		0.807 0.240 6 31572294 5 prime UTR variant G/A;C snv 0.39
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2007 2007