Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1048218
rs1048218
1.000 0.080 11 27658340 missense variant C/A snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.010 1.000 1 2008 2008
dbSNP: rs1048220
rs1048220
1.000 0.040 11 27658191 missense variant C/A snv
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
0.010 1.000 1 2019 2019
dbSNP: rs10767664
rs10767664
0.752 0.400 11 27704439 intron variant T/A snv 0.83
CUI: C0004096
Disease: Asthma
Asthma
0.020 1.000 2 2011 2016
dbSNP: rs10767664
rs10767664
0.752 0.400 11 27704439 intron variant T/A snv 0.83
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder)
0.020 1.000 2 2011 2015
dbSNP: rs10767664
rs10767664
0.752 0.400 11 27704439 intron variant T/A snv 0.83
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index
0.700 1.000 2 2010 2013
dbSNP: rs10767664
rs10767664
0.752 0.400 11 27704439 intron variant T/A snv 0.83
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 2 2010 2019
dbSNP: rs10767664
rs10767664
0.752 0.400 11 27704439 intron variant T/A snv 0.83
CUI: C0028754
Disease: Obesity
Obesity
0.020 1.000 2 2017 2017
dbSNP: rs10767664
rs10767664
0.752 0.400 11 27704439 intron variant T/A snv 0.83
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure
0.700 1.000 2 2010 2013
dbSNP: rs10767664
rs10767664
0.752 0.400 11 27704439 intron variant T/A snv 0.83
CUI: C0264408
Disease: Childhood asthma
Childhood asthma
0.010 1.000 1 2013 2013
dbSNP: rs10767664
rs10767664
0.752 0.400 11 27704439 intron variant T/A snv 0.83
CUI: C0852733
Disease: Completed Suicide
Completed Suicide
0.010 1.000 1 2015 2015
dbSNP: rs10767664
rs10767664
0.752 0.400 11 27704439 intron variant T/A snv 0.83
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.010 1.000 1 2017 2017
dbSNP: rs10767664
rs10767664
0.752 0.400 11 27704439 intron variant T/A snv 0.83
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.010 1.000 1 2014 2014
dbSNP: rs10767664
rs10767664
0.752 0.400 11 27704439 intron variant T/A snv 0.83
Diabetes Mellitus, Non-Insulin-Dependent
0.010 1.000 1 2017 2017
dbSNP: rs10767664
rs10767664
0.752 0.400 11 27704439 intron variant T/A snv 0.83
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.010 1.000 1 2014 2014
dbSNP: rs10767664
rs10767664
0.752 0.400 11 27704439 intron variant T/A snv 0.83
CUI: C0281899
Disease: Prolapsed lumbar disc
Prolapsed lumbar disc
0.010 1.000 1 2018 2018
dbSNP: rs10767664
rs10767664
0.752 0.400 11 27704439 intron variant T/A snv 0.83
CUI: C0019337
Disease: Heroin Dependence
Heroin Dependence
0.010 1.000 1 2016 2016
dbSNP: rs10767664
rs10767664
0.752 0.400 11 27704439 intron variant T/A snv 0.83
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.010 1.000 1 2014 2014
dbSNP: rs10767664
rs10767664
0.752 0.400 11 27704439 intron variant T/A snv 0.83
CUI: C0043144
Disease: Wheezing
Wheezing
0.010 1.000 1 2016 2016
dbSNP: rs10835210
rs10835210
0.882 0.040 11 27674363 intron variant C/A;G snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.020 1.000 2 2016 2016
dbSNP: rs10835210
rs10835210
0.882 0.040 11 27674363 intron variant C/A;G snv
CUI: C0003469
Disease: Anxiety Disorders
Anxiety Disorders
0.010 1.000 1 2018 2018
dbSNP: rs10835210
rs10835210
0.882 0.040 11 27674363 intron variant C/A;G snv
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
0.010 1.000 1 2009 2009
dbSNP: rs10835210
rs10835210
0.882 0.040 11 27674363 intron variant C/A;G snv
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.010 1.000 1 2012 2012
dbSNP: rs10835211
rs10835211
1.000 0.080 11 27679818 intron variant G/A snv 0.19
CUI: C0011168
Disease: Deglutition Disorders
Deglutition Disorders
0.010 1.000 1 2015 2015
dbSNP: rs10835211
rs10835211
1.000 0.080 11 27679818 intron variant G/A snv 0.19
CUI: C0028754
Disease: Obesity
Obesity
0.700 1.000 1 2013 2013
dbSNP: rs10835211
rs10835211
1.000 0.080 11 27679818 intron variant G/A snv 0.19
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2019 2019