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: rs4765905
rs4765905
0.827 0.040 12 2240418 intron variant G/A;C snv
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
Mental Disorders 0.710 1.000 2 2011 2016
dbSNP: rs4765914
rs4765914
0.925 0.040 12 2311211 intron variant T/C;G snv
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
Mental Disorders 0.800 1.000 2 2013 2019
dbSNP: rs758117
rs758117
1.000 0.040 12 2404143 intron variant C/T snv 0.23
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.700 1.000 2 2017 2019
dbSNP: rs786205748
rs786205748
1.000 0.120 12 2566465 missense variant C/T snv
CUI: C0023976
Disease: Long QT Syndrome
Long QT Syndrome
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases 0.710 1.000 2 2015 2019
dbSNP: rs7972947
rs7972947
1.000 0.040 12 2061267 intron variant C/A;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.700 1.000 2 2011 2013
dbSNP: rs1006737
rs1006737
0.695 0.120 12 2236129 intron variant G/A snv 0.36
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
Mental Disorders 0.010 < 0.001 1 2016 2016
dbSNP: rs1006737
rs1006737
0.695 0.120 12 2236129 intron variant G/A snv 0.36
CUI: C0154409
Disease: Recurrent major depressive episodes
Recurrent major depressive episodes
Mental Disorders 0.010 1.000 1 2010 2010
dbSNP: rs1006737
rs1006737
0.695 0.120 12 2236129 intron variant G/A snv 0.36
CUI: C0036572
Disease: Seizures
Seizures
Pathological Conditions, Signs and Symptoms; Nervous System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs1006737
rs1006737
0.695 0.120 12 2236129 intron variant G/A snv 0.36
CUI: C0003467
Disease: Anxiety
Anxiety
Behavior and Behavior Mechanisms 0.010 1.000 1 2011 2011
dbSNP: rs1006737
rs1006737
0.695 0.120 12 2236129 intron variant G/A snv 0.36
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders
Nervous System Diseases 0.010 < 0.001 1 2011 2011
dbSNP: rs1006737
rs1006737
0.695 0.120 12 2236129 intron variant G/A snv 0.36
CUI: C0036363
Disease: Schizotypal Personality Disorder
Schizotypal Personality Disorder
Mental Disorders 0.010 1.000 1 2019 2019
dbSNP: rs1006737
rs1006737
0.695 0.120 12 2236129 intron variant G/A snv 0.36
CUI: C0747249
Disease: Paranoid ideation
Paranoid ideation
0.010 1.000 1 2011 2011
dbSNP: rs1006737
rs1006737
0.695 0.120 12 2236129 intron variant G/A snv 0.36
CUI: C0154723
Disease: Migraine with Aura
Migraine with Aura
Nervous System Diseases 0.010 < 0.001 1 2011 2011
dbSNP: rs1006737
rs1006737
0.695 0.120 12 2236129 intron variant G/A snv 0.36
CUI: C0338480
Disease: Common Migraine
Common Migraine
Nervous System Diseases 0.010 < 0.001 1 2011 2011
dbSNP: rs1006737
rs1006737
0.695 0.120 12 2236129 intron variant G/A snv 0.36
Attention deficit hyperactivity disorder
Mental Disorders 0.800 1.000 1 2013 2013
dbSNP: rs1006737
rs1006737
0.695 0.120 12 2236129 intron variant G/A snv 0.36
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
Mental Disorders 0.010 1.000 1 2015 2015
dbSNP: rs1006737
rs1006737
0.695 0.120 12 2236129 intron variant G/A snv 0.36
Child Development Disorders, Pervasive
Mental Disorders 0.700 1.000 1 2013 2013
dbSNP: rs1006737
rs1006737
0.695 0.120 12 2236129 intron variant G/A snv 0.36
CUI: C0917801
Disease: Sleeplessness
Sleeplessness
Nervous System Diseases; Mental Disorders 0.010 1.000 1 2010 2010
dbSNP: rs1006737
rs1006737
0.695 0.120 12 2236129 intron variant G/A snv 0.36
CUI: C0006012
Disease: Borderline Personality Disorder
Borderline Personality Disorder
Mental Disorders 0.010 1.000 1 2014 2014
dbSNP: rs1006737
rs1006737
0.695 0.120 12 2236129 intron variant G/A snv 0.36
CUI: C0003469
Disease: Anxiety Disorders
Anxiety Disorders
Mental Disorders 0.010 1.000 1 2011 2011
dbSNP: rs1016388
rs1016388
1.000 0.040 12 2212702 intron variant A/T snv 0.53
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.010 1.000 1 2015 2015
dbSNP: rs1024582
rs1024582
1.000 0.040 12 2293080 intron variant A/G;T snv
Child Development Disorders, Pervasive
Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs1034936
rs1034936
0.882 0.080 12 2551994 intron variant C/T snv 0.61
CUI: C0085762
Disease: Alcohol abuse
Alcohol abuse
Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2020 2020
dbSNP: rs1034936
rs1034936
0.882 0.080 12 2551994 intron variant C/T snv 0.61
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic
Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2020 2020
dbSNP: rs1034936
rs1034936
0.882 0.080 12 2551994 intron variant C/T snv 0.61
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
Mental Disorders 0.010 1.000 1 2020 2020