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: rs2535629
rs2535629
0.827 0.040 3 52799203 intron variant G/A;C snv
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
Mental Disorders 0.820 1.000 4 2013 2019
dbSNP: rs2535629
rs2535629
0.827 0.040 3 52799203 intron variant G/A;C snv
Attention deficit hyperactivity disorder
Mental Disorders 0.810 1.000 2 2013 2015
dbSNP: rs4687552
rs4687552
0.925 0.080 3 52804386 non coding transcript exon variant T/C snv 0.33
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.800 1.000 1 2013 2013
dbSNP: rs2535629
rs2535629
0.827 0.040 3 52799203 intron variant G/A;C snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.720 0.750 4 2013 2019
dbSNP: rs3617
rs3617
1.000 0.040 3 52799789 missense variant C/A snv 0.48 0.54
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.700 1.000 3 2017 2019
dbSNP: rs2535629
rs2535629
0.827 0.040 3 52799203 intron variant G/A;C snv
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
Mental Disorders 0.700 1.000 2 2013 2019
dbSNP: rs115714636
rs115714636
3 52796511 missense variant A/G snv 1.6E-03 6.4E-03
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption
Behavior and Behavior Mechanisms 0.700 1.000 1 2013 2013
dbSNP: rs138014257
rs138014257
3 52808491 intron variant C/T snv 1.1E-02
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs2240919
rs2240919
3 52797685 intron variant C/G snv 0.26
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2014 2014
dbSNP: rs2240920
rs2240920
3 52796993 intron variant C/T snv 0.34
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2017 2017
dbSNP: rs2286797
rs2286797
1.000 0.080 3 52795617 synonymous variant G/A snv 4.5E-02 1.7E-02
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 1 2007 2007
dbSNP: rs2535629
rs2535629
0.827 0.040 3 52799203 intron variant G/A;C snv
Child Development Disorders, Pervasive
Mental Disorders 0.700 1.000 1 2013 2013
dbSNP: rs3617
rs3617
1.000 0.040 3 52799789 missense variant C/A snv 0.48 0.54
Child Development Disorders, Pervasive
Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs3617
rs3617
1.000 0.040 3 52799789 missense variant C/A snv 0.48 0.54
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2016 2016
dbSNP: rs4687552
rs4687552
0.925 0.080 3 52804386 non coding transcript exon variant T/C snv 0.33
CUI: C0003467
Disease: Anxiety
Anxiety
Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs736408
rs736408
1.000 0.040 3 52801338 intron variant C/T snv 0.47
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
Mental Disorders 0.700 1.000 1 2013 2013
dbSNP: rs2535629
rs2535629
0.827 0.040 3 52799203 intron variant G/A;C snv
CUI: C0086132
Disease: Depressive Symptoms
Depressive Symptoms
Behavior and Behavior Mechanisms 0.010 < 0.001 1 2018 2018
dbSNP: rs2535629
rs2535629
0.827 0.040 3 52799203 intron variant G/A;C snv
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
Behavior and Behavior Mechanisms 0.010 1.000 1 2014 2014
dbSNP: rs2535629
rs2535629
0.827 0.040 3 52799203 intron variant G/A;C snv
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
Mental Disorders 0.010 1.000 1 2019 2019
dbSNP: rs2535629
rs2535629
0.827 0.040 3 52799203 intron variant G/A;C snv
CUI: C0004936
Disease: Mental disorders
Mental disorders
Mental Disorders 0.010 1.000 1 2014 2014
dbSNP: rs736408
rs736408
1.000 0.040 3 52801338 intron variant C/T snv 0.47
CUI: C0086132
Disease: Depressive Symptoms
Depressive Symptoms
Behavior and Behavior Mechanisms 0.010 < 0.001 1 2018 2018