Source: BEFREE

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: rs10994336
rs10994336
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.900 0.933 13 2008 2018
dbSNP: rs10994336
rs10994336
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
0.710 1.000 1 2011 2011
dbSNP: rs10994336
rs10994336
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.040 1.000 4 2011 2016
dbSNP: rs10994336
rs10994336
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02
CUI: C0006012
Disease: Borderline Personality Disorder
Borderline Personality Disorder
0.020 0.500 2 2011 2014
dbSNP: rs10994336
rs10994336
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02
CUI: C0006287
Disease: Bronchopulmonary Dysplasia
Bronchopulmonary Dysplasia
0.020 0.500 2 2011 2014
dbSNP: rs10994336
rs10994336
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02
CUI: C0525045
Disease: Mood Disorders
Mood Disorders
0.010 1.000 1 2014 2014
dbSNP: rs10994336
rs10994336
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02
CUI: C0041696
Disease: Unipolar Depression
Unipolar Depression
0.010 1.000 1 2011 2011
dbSNP: rs10994336
rs10994336
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders
0.010 < 0.001 1 2011 2011
dbSNP: rs10994336
rs10994336
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02
CUI: C0338480
Disease: Common Migraine
Common Migraine
0.010 < 0.001 1 2011 2011
dbSNP: rs10994336
rs10994336
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02
CUI: C0004936
Disease: Mental disorders
Mental disorders
0.010 1.000 1 2015 2015
dbSNP: rs10994336
rs10994336
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.010 1.000 1 2015 2015
dbSNP: rs10994336
rs10994336
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02
CUI: C0154723
Disease: Migraine with Aura
Migraine with Aura
0.010 < 0.001 1 2011 2011