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: 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: rs1720825
rs1720825 		3 138389241 intron variant A/G;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2017 2018
dbSNP: rs1199334
rs1199334 		3 138372298 intron variant A/C;G;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs1199337
rs1199337 		1.000 0.040 3 138369222 intron variant G/C snv 0.19
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs1209710
rs1209710 		1.000 0.080 3 138387856 intron variant C/T snv 0.82
CUI: C0027404
Disease: Narcolepsy
Narcolepsy 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2009 2009
dbSNP: rs1308362
rs1308362 		3 138385085 intron variant A/G;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2017 2017
dbSNP: rs1308362
rs1308362 		3 138385085 intron variant A/G;T snv
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement 		0.700 1.000 1 2017 2017
dbSNP: rs1375027098
rs1375027098 		1.000 0.160 3 138372947 frameshift variant G/- delins 7.0E-06
CUI: C0028326
Disease: Noonan Syndrome
Noonan Syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases 0.010 1.000 1 2019 2019
dbSNP: rs139016349
rs139016349 		1.000 0.040 3 138380319 intron variant -/CTT delins 0.21
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 1 2017 2017
dbSNP: rs140371629
rs140371629 		3 138348474 intron variant G/C snv 4.6E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs1678443
rs1678443 		3 138378692 intron variant C/A snv 8.6E-02
CUI: C0429087
Disease: Electrocardiogram: P-R interval
Electrocardiogram: P-R interval 		0.700 1.000 1 2013 2013
dbSNP: rs1720819
rs1720819 		1.000 0.040 3 138381697 intron variant T/G snv 0.18
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 1.000 1 2013 2013
dbSNP: rs1720825
rs1720825 		3 138389241 intron variant A/G;T snv
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement 		0.700 1.000 1 2017 2017
dbSNP: rs185244
rs185244 		1.000 0.040 3 138374047 intron variant C/T snv 0.19
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs2306374
rs2306374 		0.925 0.040 3 138401110 intron variant T/C snv 0.12
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 1 2013 2013
dbSNP: rs2306374
rs2306374 		0.925 0.040 3 138401110 intron variant T/C snv 0.12
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.800 1.000 1 2011 2011
dbSNP: rs253662
rs253662 		1.000 0.040 3 138378471 intron variant T/C snv 0.84
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 1.000 1 2013 2013
dbSNP: rs253664
rs253664 		3 138394511 intron variant T/C snv 0.85
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2015 2015
dbSNP: rs3732837
rs3732837 		1.000 0.040 3 138403078 3 prime UTR variant A/G;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs40593
rs40593 		1.000 0.080 3 138403939 3 prime UTR variant A/G snv 4.0E-02
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2019 2019
dbSNP: rs6782181
rs6782181 		0.851 0.160 3 138386212 intron variant G/A;C snv
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2013 2013
dbSNP: rs6782181
rs6782181 		0.851 0.160 3 138386212 intron variant G/A;C snv
CUI: C0020443
Disease: Hypercholesterolemia
Hypercholesterolemia 		Nutritional and Metabolic Diseases 0.010 1.000 1 2013 2013
dbSNP: rs6782181
rs6782181 		0.851 0.160 3 138386212 intron variant G/A;C snv
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia 		Nutritional and Metabolic Diseases 0.010 1.000 1 2013 2013
dbSNP: rs6782181
rs6782181 		0.851 0.160 3 138386212 intron variant G/A;C snv
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2019 2019