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: rs3125
rs3125
HTR2A
0.925 0.080 13 46834716 3 prime UTR variant C/G;T snv
CUI: C0011581
Disease: Depressive disorder
Depressive disorder 		0.010 1.000 1 2019 2019
dbSNP: rs3125
rs3125
HTR2A
0.925 0.080 13 46834716 3 prime UTR variant C/G;T snv
CUI: C0011570
Disease: Mental Depression
Mental Depression 		0.010 1.000 1 2019 2019
dbSNP: rs3125
rs3125
HTR2A
0.925 0.080 13 46834716 3 prime UTR variant C/G;T snv
CUI: C0344315
Disease: Depressed mood
Depressed mood 		0.010 1.000 1 2019 2019
dbSNP: rs3125
rs3125
HTR2A
0.925 0.080 13 46834716 3 prime UTR variant C/G;T snv
CUI: C0154575
Disease: Rumination Disorders
Rumination Disorders 		0.010 1.000 1 2019 2019
dbSNP: rs6314
rs6314
HTR2A
0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.080 1.000 8 1998 2017
dbSNP: rs6314
rs6314
HTR2A
0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		0.030 0.667 3 2000 2007
dbSNP: rs6314
rs6314
HTR2A
0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders 		0.020 1.000 2 2014 2014
dbSNP: rs6314
rs6314
HTR2A
0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02
CUI: C3714760
Disease: Drug-induced tardive dyskinesia
Drug-induced tardive dyskinesia 		0.020 0.500 2 2001 2005
dbSNP: rs6314
rs6314
HTR2A
0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02
CUI: C0686347
Disease: Tardive Dyskinesia
Tardive Dyskinesia 		0.020 0.500 2 2001 2005
dbSNP: rs6314
rs6314
HTR2A
0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.020 1.000 2 2001 2014
dbSNP: rs6314
rs6314
HTR2A
0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02
CUI: C0036337
Disease: Schizoaffective Disorder
Schizoaffective Disorder 		0.010 1.000 1 2010 2010
dbSNP: rs6314
rs6314
HTR2A
0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02
CUI: C0853193
Disease: Bipolar I disorder
Bipolar I disorder 		0.010 1.000 1 2003 2003
dbSNP: rs6314
rs6314
HTR2A
0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.010 1.000 1 2013 2013
dbSNP: rs6314
rs6314
HTR2A
0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02
CUI: C0041696
Disease: Unipolar Depression
Unipolar Depression 		0.010 1.000 1 2001 2001
dbSNP: rs6314
rs6314
HTR2A
0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02
CUI: C0028754
Disease: Obesity
Obesity 		0.010 1.000 1 2013 2013
dbSNP: rs6314
rs6314
HTR2A
0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02
CUI: C0086132
Disease: Depressive Symptoms
Depressive Symptoms 		0.010 1.000 1 2014 2014
dbSNP: rs6314
rs6314
HTR2A
0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02
CUI: C0013384
Disease: Dyskinetic syndrome
Dyskinetic syndrome 		0.010 1.000 1 2012 2012
dbSNP: rs6314
rs6314
HTR2A
0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02
CUI: C0014556
Disease: Epilepsy, Temporal Lobe
Epilepsy, Temporal Lobe 		0.010 1.000 1 2012 2012
dbSNP: rs6314
rs6314
HTR2A
0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02
CUI: C0011570
Disease: Mental Depression
Mental Depression 		0.010 < 0.001 1 2014 2014
dbSNP: rs6314
rs6314
HTR2A
0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02
CUI: C4694057
Disease: Taq1A POLYMORPHISM
Taq1A POLYMORPHISM 		0.010 1.000 1 2007 2007
dbSNP: rs6314
rs6314
HTR2A
0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02
CUI: C0011581
Disease: Depressive disorder
Depressive disorder 		0.010 < 0.001 1 2014 2014
dbSNP: rs6314
rs6314
HTR2A
0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02
CUI: C0524528
Disease: Pervasive Development Disorder
Pervasive Development Disorder 		0.010 1.000 1 2014 2014
dbSNP: rs6314
rs6314
HTR2A
0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.010 1.000 1 2002 2002
dbSNP: rs6314
rs6314
HTR2A
0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02
CUI: C0344315
Disease: Depressed mood
Depressed mood 		0.010 < 0.001 1 2014 2014
dbSNP: rs6314
rs6314
HTR2A
0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02
CUI: C0027849
Disease: Neuroleptic Malignant Syndrome
Neuroleptic Malignant Syndrome 		0.010 1.000 1 1998 1998