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: rs6318
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		0.040 1.000 4 2001 2018
dbSNP: rs6318
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		0.030 0.333 3 1999 2003
dbSNP: rs6318
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv
CUI: C0344315
Disease: Depressed mood
Depressed mood 		0.030 1.000 3 2012 2018
dbSNP: rs6318
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv
CUI: C0004936
Disease: Mental disorders
Mental disorders 		0.030 0.667 3 1999 2015
dbSNP: rs6318
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior 		0.030 0.667 3 1999 2015
dbSNP: rs6318
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv
CUI: C0011581
Disease: Depressive disorder
Depressive disorder 		0.030 1.000 3 2012 2018
dbSNP: rs6318
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv
CUI: C0011570
Disease: Mental Depression
Mental Depression 		0.030 1.000 3 2012 2018
dbSNP: rs6318
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv
CUI: C0154723
Disease: Migraine with Aura
Migraine with Aura 		0.020 0.500 2 2004 2007
dbSNP: rs6318
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		0.020 0.500 2 2004 2007
dbSNP: rs6318
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv
CUI: C0086132
Disease: Depressive Symptoms
Depressive Symptoms 		0.020 1.000 2 2014 2018
dbSNP: rs6318
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv
CUI: C0028754
Disease: Obesity
Obesity 		0.010 < 0.001 1 1997 1997
dbSNP: rs6318
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv
CUI: C0730557
Disease: Emotional abuse
Emotional abuse 		0.010 1.000 1 2015 2015
dbSNP: rs6318
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 2013 2013
dbSNP: rs6318
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv
CUI: C1970945
Disease: MAJOR AFFECTIVE DISORDER 6
MAJOR AFFECTIVE DISORDER 6 		0.010 1.000 1 1996 1996
dbSNP: rs6318
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv
CUI: C0085159
Disease: Seasonal Affective Disorder
Seasonal Affective Disorder 		0.010 1.000 1 2005 2005
dbSNP: rs6318
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv
CUI: C1852197
Disease: MAJOR AFFECTIVE DISORDER 1
MAJOR AFFECTIVE DISORDER 1 		0.010 1.000 1 1996 1996
dbSNP: rs6318
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv
CUI: C3714760
Disease: Drug-induced tardive dyskinesia
Drug-induced tardive dyskinesia 		0.010 1.000 1 2009 2009
dbSNP: rs6318
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.010 1.000 1 1998 1998
dbSNP: rs6318
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv
CUI: C0871388
Disease: social stress
social stress 		0.010 1.000 1 2016 2016
dbSNP: rs6318
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		0.010 < 0.001 1 2003 2003
dbSNP: rs6318
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv
CUI: C0020514
Disease: Hyperprolactinemia
Hyperprolactinemia 		0.010 1.000 1 2015 2015
dbSNP: rs6318
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv
CUI: C0003469
Disease: Anxiety Disorders
Anxiety Disorders 		0.010 1.000 1 2017 2017
dbSNP: rs6318
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv
CUI: C2700438
Disease: MAJOR AFFECTIVE DISORDER 7
MAJOR AFFECTIVE DISORDER 7 		0.010 1.000 1 1996 1996
dbSNP: rs6318
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.010 1.000 1 2013 2013
dbSNP: rs6318
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv
CUI: C0154409
Disease: Recurrent major depressive episodes
Recurrent major depressive episodes 		0.010 1.000 1 2001 2001