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: 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: 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: rs6782181
rs6782181
0.851 0.160 3 138386212 intron variant G/A;C snv
CUI: C0018498
Disease: Hair Color
Hair Color
0.700 1.000 1 2018 2018
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: 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
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
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: 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