PLG, plasminogen, 5340

N. diseases: 586; N. variants: 34
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: rs779647096
rs779647096 		0.882 0.080 6 160718313 synonymous variant T/C snv 1.2E-05 7.0E-06
CUI: C0333205
Disease: Mural thrombus
Mural thrombus 		Cardiovascular Diseases 0.010 1.000 1 2002 2002
dbSNP: rs779647096
rs779647096 		0.882 0.080 6 160718313 synonymous variant T/C snv 1.2E-05 7.0E-06
CUI: C1260883
Disease: Mural thrombus of heart
Mural thrombus of heart 		Cardiovascular Diseases 0.010 1.000 1 2002 2002
dbSNP: rs9458010
rs9458010 		6 160704387 intron variant T/C snv 0.38
CUI: C1096202
Disease: Lipoprotein (a) measurement
Lipoprotein (a) measurement 		0.700 1.000 1 2017 2017
dbSNP: rs4252120
rs4252120 		0.827 0.080 6 160722576 intron variant T/C;G snv 0.21
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.710 1.000 2 2013 2015
dbSNP: rs4252120
rs4252120 		0.827 0.080 6 160722576 intron variant T/C;G snv 0.21
CUI: C0031106
Disease: Aggressive Periodontitis
Aggressive Periodontitis 		Stomatognathic Diseases 0.020 0.500 2 2015 2017
dbSNP: rs4252120
rs4252120 		0.827 0.080 6 160722576 intron variant T/C;G snv 0.21
CUI: C0001342
Disease: Acute periodontitis
Acute periodontitis 		Stomatognathic Diseases 0.020 0.500 2 2015 2017
dbSNP: rs4252120
rs4252120 		0.827 0.080 6 160722576 intron variant T/C;G snv 0.21
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs4252120
rs4252120 		0.827 0.080 6 160722576 intron variant T/C;G snv 0.21
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs770198253
rs770198253 		1.000 0.120 6 160713018 missense variant T/C;G snv 4.0E-06; 4.0E-06; 4.0E-06
CUI: C1968804
Disease: Plasminogen Deficiency, Type I
Plasminogen Deficiency, Type I 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases 0.700 0
dbSNP: rs147402310
rs147402310 		6 160742498 intron variant T/G snv 2.4E-02
CUI: C1096202
Disease: Lipoprotein (a) measurement
Lipoprotein (a) measurement 		0.700 1.000 1 2017 2017
dbSNP: rs4252109
rs4252109 		6 160716631 intron variant T/G snv 0.21 0.23
CUI: C1096202
Disease: Lipoprotein (a) measurement
Lipoprotein (a) measurement 		0.700 1.000 1 2017 2017