TFPI, tissue factor pathway inhibitor, 7035

N. diseases: 230; N. variants: 6
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: rs4140885
rs4140885 		2 187468337 intron variant G/A snv 0.35
CUI: C0018810
Disease: heart rate
heart rate 		0.800 1.000 1 2013 2013
dbSNP: rs8176433
rs8176433 		2 187500098 intron variant C/G snv 1.2E-02
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs8176433
rs8176433 		2 187500098 intron variant C/G snv 1.2E-02
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs8176433
rs8176433 		2 187500098 intron variant C/G snv 1.2E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs8176445
rs8176445 		2 187498080 intron variant T/C snv 8.7E-03
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs8176445
rs8176445 		2 187498080 intron variant T/C snv 8.7E-03
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs8176445
rs8176445 		2 187498080 intron variant T/C snv 8.7E-03
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs8176445
rs8176445 		2 187498080 intron variant T/C snv 8.7E-03
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs5940
rs5940 		0.882 0.080 2 187466977 missense variant C/T snv 1.3E-02 1.4E-02
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 1999 1999
dbSNP: rs5940
rs5940 		0.882 0.080 2 187466977 missense variant C/T snv 1.3E-02 1.4E-02
CUI: C0149871
Disease: Deep Vein Thrombosis
Deep Vein Thrombosis 		Cardiovascular Diseases 0.010 < 0.001 1 2001 2001
dbSNP: rs5940
rs5940 		0.882 0.080 2 187466977 missense variant C/T snv 1.3E-02 1.4E-02
CUI: C0948089
Disease: Acute Coronary Syndrome
Acute Coronary Syndrome 		Cardiovascular Diseases 0.010 1.000 1 1999 1999
dbSNP: rs6434222
rs6434222 		1.000 0.040 2 187547517 non coding transcript exon variant T/A snv 0.19
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs7586970
rs7586970 		0.925 0.040 2 187478770 missense variant T/C;G snv 0.29
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs7586970
rs7586970 		0.925 0.040 2 187478770 missense variant T/C;G snv 0.29
CUI: C0149871
Disease: Deep Vein Thrombosis
Deep Vein Thrombosis 		Cardiovascular Diseases 0.010 1.000 1 2009 2009