rs1234313, TNFSF4

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.
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.807 0.400 1 173197108 intron variant A/G snv 0.72 0.010 1.000 1 2017 2017
Cerebral arterial thrombosis
CUI: C0795687
Disease: Cerebral arterial thrombosis
9 0.807 0.400 1 173197108 intron variant A/G snv 0.72 0.010 1.000 1 2019 2019
Large-artery atherosclerosis (embolus/thrombosis)
CUI: C4699512
Disease: Large-artery atherosclerosis (embolus/thrombosis)
35 0.807 0.400 1 173197108 intron variant A/G snv 0.72 0.010 1.000 1 2019 2019
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.807 0.400 1 173197108 intron variant A/G snv 0.72 0.010 1.000 1 2015 2015
Primary biliary cirrhosis
CUI: C0008312
Disease: Primary biliary cirrhosis
667 0.807 0.400 1 173197108 intron variant A/G snv 0.72 0.010 1.000 1 2013 2013
Primary Sjögren's syndrome
CUI: C0151449
Disease: Primary Sjögren's syndrome
42 0.807 0.400 1 173197108 intron variant A/G snv 0.72 0.010 1.000 1 2013 2013