MRAS, muscle RAS oncogene homolog, 22808

N. diseases: 113; N. variants: 22
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: rs730158
rs730158 		3 138359356 intron variant T/A;C snv
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs751357
rs751357 		1.000 0.080 3 138359313 intron variant T/C snv 0.65
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2019 2019
dbSNP: rs9818870
rs9818870 		0.807 0.200 3 138403280 3 prime UTR variant C/A;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.740 0.600 5 2011 2019
dbSNP: rs9818870
rs9818870 		0.807 0.200 3 138403280 3 prime UTR variant C/A;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.800 1.000 3 2009 2014
dbSNP: rs9818870
rs9818870 		0.807 0.200 3 138403280 3 prime UTR variant C/A;T snv
CUI: C0018799
Disease: Heart Diseases
Heart Diseases 		Cardiovascular Diseases 0.010 < 0.001 1 2011 2011
dbSNP: rs9818870
rs9818870 		0.807 0.200 3 138403280 3 prime UTR variant C/A;T snv
CUI: C0948089
Disease: Acute Coronary Syndrome
Acute Coronary Syndrome 		Cardiovascular Diseases 0.010 < 0.001 1 2017 2017
dbSNP: rs9818870
rs9818870 		0.807 0.200 3 138403280 3 prime UTR variant C/A;T snv
CUI: C0856169
Disease: Endothelial dysfunction
Endothelial dysfunction 		0.010 < 0.001 1 2015 2015
dbSNP: rs9818870
rs9818870 		0.807 0.200 3 138403280 3 prime UTR variant C/A;T snv
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		Cardiovascular Diseases 0.010 < 0.001 1 2015 2015
dbSNP: rs9818870
rs9818870 		0.807 0.200 3 138403280 3 prime UTR variant C/A;T snv
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.700 1.000 1 2019 2019
dbSNP: rs9818870
rs9818870 		0.807 0.200 3 138403280 3 prime UTR variant C/A;T snv
CUI: C0742343
Disease: Acute Chest Syndrome
Acute Chest Syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Hemic and Lymphatic Diseases 0.010 < 0.001 1 2017 2017
dbSNP: rs9818870
rs9818870 		0.807 0.200 3 138403280 3 prime UTR variant C/A;T snv
CUI: C1842247
Disease: CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 1 2013 2013
dbSNP: rs9864898
rs9864898 		3 138392909 intron variant C/T snv 0.12
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2017 2017
dbSNP: rs9864898
rs9864898 		3 138392909 intron variant C/T snv 0.12
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2017 2017
dbSNP: rs9872754
rs9872754 		3 138399143 intron variant C/T snv 0.12
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019