Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs3850641
rs3850641
TNFSF4
0.716 0.400 1 173206693 intron variant A/G snv 0.14
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.060 1.000 6 2005 2019
dbSNP: rs3850641
rs3850641
TNFSF4
0.716 0.400 1 173206693 intron variant A/G snv 0.14
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.020 1.000 2 2018 2019
dbSNP: rs3850641
rs3850641
TNFSF4
0.716 0.400 1 173206693 intron variant A/G snv 0.14
CUI: C0742343
Disease: Acute Chest Syndrome
Acute Chest Syndrome 		0.020 1.000 2 2011 2019
dbSNP: rs3850641
rs3850641
TNFSF4
0.716 0.400 1 173206693 intron variant A/G snv 0.14
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		0.010 1.000 1 2013 2013
dbSNP: rs3850641
rs3850641
TNFSF4
0.716 0.400 1 173206693 intron variant A/G snv 0.14
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.010 < 0.001 1 2018 2018
dbSNP: rs3850641
rs3850641
TNFSF4
0.716 0.400 1 173206693 intron variant A/G snv 0.14
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.010 1.000 1 2012 2012
dbSNP: rs3850641
rs3850641
TNFSF4
0.716 0.400 1 173206693 intron variant A/G snv 0.14
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		0.010 1.000 1 2018 2018
dbSNP: rs3850641
rs3850641
TNFSF4
0.716 0.400 1 173206693 intron variant A/G snv 0.14
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.010 1.000 1 2008 2008
dbSNP: rs3850641
rs3850641
TNFSF4
0.716 0.400 1 173206693 intron variant A/G snv 0.14
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.010 1.000 1 2012 2012
dbSNP: rs3850641
rs3850641
TNFSF4
0.716 0.400 1 173206693 intron variant A/G snv 0.14
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		0.010 1.000 1 2013 2013
dbSNP: rs3850641
rs3850641
TNFSF4
0.716 0.400 1 173206693 intron variant A/G snv 0.14
CUI: C0677607
Disease: Hashimoto Disease
Hashimoto Disease 		0.010 1.000 1 2016 2016
dbSNP: rs3850641
rs3850641
TNFSF4
0.716 0.400 1 173206693 intron variant A/G snv 0.14
CUI: C0023817
Disease: Hyperlipoproteinemia Type I
Hyperlipoproteinemia Type I 		0.010 1.000 1 2013 2013
dbSNP: rs3850641
rs3850641
TNFSF4
0.716 0.400 1 173206693 intron variant A/G snv 0.14
CUI: C0948089
Disease: Acute Coronary Syndrome
Acute Coronary Syndrome 		0.010 1.000 1 2019 2019
dbSNP: rs3850641
rs3850641
TNFSF4
0.716 0.400 1 173206693 intron variant A/G snv 0.14
CUI: C0007785
Disease: Cerebral Infarction
Cerebral Infarction 		0.010 1.000 1 2013 2013
dbSNP: rs3850641
rs3850641
TNFSF4
0.716 0.400 1 173206693 intron variant A/G snv 0.14
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.010 1.000 1 2016 2016
dbSNP: rs3850641
rs3850641
TNFSF4
0.716 0.400 1 173206693 intron variant A/G snv 0.14
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.010 1.000 1 2012 2012
dbSNP: rs3850641
rs3850641
TNFSF4
0.716 0.400 1 173206693 intron variant A/G snv 0.14
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		0.010 1.000 1 2018 2018