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: rs774229224
rs774229224 		0.882 0.160 6 160706454 missense variant C/A;G snv 4.0E-06; 4.0E-06
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 1998 1998
dbSNP: rs774229224
rs774229224 		0.882 0.160 6 160706454 missense variant C/A;G snv 4.0E-06; 4.0E-06
CUI: C4552766
Disease: Miscarriage
Miscarriage 		Female Urogenital Diseases and Pregnancy Complications 0.010 < 0.001 1 2007 2007
dbSNP: rs774229224
rs774229224 		0.882 0.160 6 160706454 missense variant C/A;G snv 4.0E-06; 4.0E-06
CUI: C0007820
Disease: Cerebrovascular Disorders
Cerebrovascular Disorders 		Nervous System Diseases; Cardiovascular Diseases 0.010 < 0.001 1 1998 1998
dbSNP: rs774484989
rs774484989 		1.000 0.040 6 160739148 missense variant A/G snv 4.0E-06
CUI: C4552766
Disease: Miscarriage
Miscarriage 		Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2013 2013
dbSNP: rs778686781
rs778686781 		1.000 0.080 6 160718329 missense variant T/C snv 4.0E-06
CUI: C1260903
Disease: Dysfibrinogenemia
Dysfibrinogenemia 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases 0.010 1.000 1 2000 2000
dbSNP: rs779290753
rs779290753 		1.000 0.080 6 160706424 missense variant G/A snv 8.0E-06
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.010 1.000 1 2008 2008
dbSNP: rs779647096
rs779647096 		0.882 0.080 6 160718313 synonymous variant T/C snv 1.2E-05 7.0E-06
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2003 2003
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: rs783147
rs783147 		1.000 0.040 6 160716958 intron variant G/A snv 0.39
CUI: C0011847
Disease: Diabetes
Diabetes 		Endocrine System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs783147
rs783147 		1.000 0.040 6 160716958 intron variant G/A snv 0.39
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2011 2011