MYH11, myosin heavy chain 11, 4629

N. diseases: 161; N. variants: 25
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: rs9922682
rs9922682
1.000 0.040 16 15852921 intron variant C/T snv 0.18
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs9933417
rs9933417
1.000 0.040 16 15854775 intron variant C/T snv 0.19
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs150759461
rs150759461
16 15778831 missense variant G/A snv 1.7E-03 1.7E-03
CUI: C0003493
Disease: Aortic Diseases
Aortic Diseases
Cardiovascular Diseases 0.020 1.000 2 2018 2018
dbSNP: rs3915499
rs3915499
16 15816886 intron variant G/A snv 0.37
CUI: C1821417
Disease: RESTING HEART RATE
RESTING HEART RATE
0.700 1.000 2 2016 2018
dbSNP: rs216158
rs216158
1.000 0.040 16 15823981 intron variant C/G snv 0.52
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs9972711
rs9972711
1.000 0.040 16 15808733 intron variant A/G;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs11130
rs11130
1.000 0.040 16 15724453 3 prime UTR variant G/A;C snv 0.56; 4.0E-06
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs11130
rs11130
1.000 0.040 16 15724453 3 prime UTR variant G/A;C snv 0.56; 4.0E-06
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs3915499
rs3915499
16 15816886 intron variant G/A snv 0.37
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2019 2019
dbSNP: rs730880147
rs730880147
1.000 16 15726938 inframe deletion CTT/- delins 4.8E-05 1.4E-05
Familial thoracic aortic aneurysm and aortic dissection
0.700 1.000 1 2019 2019