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: rs1344706
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.900 0.873 62 2008 2019
dbSNP: rs1344706
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		0.100 0.867 15 2011 2020
dbSNP: rs1344706
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv
CUI: C0033975
Disease: Psychotic Disorders
Psychotic Disorders 		0.100 1.000 10 2011 2018
dbSNP: rs1344706
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv
CUI: C0349204
Disease: Nonorganic psychosis
Nonorganic psychosis 		0.090 1.000 9 2011 2015
dbSNP: rs1344706
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		0.020 1.000 2 2011 2017
dbSNP: rs1344706
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv
CUI: C0019337
Disease: Heroin Dependence
Heroin Dependence 		0.010 1.000 1 2015 2015
dbSNP: rs1344706
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv
CUI: C0036572
Disease: Seizures
Seizures 		0.010 1.000 1 2015 2015
dbSNP: rs1344706
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.010 1.000 1 2012 2012
dbSNP: rs1344706
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv
CUI: C0041671
Disease: Attention Deficit Disorder
Attention Deficit Disorder 		0.010 1.000 1 2019 2019
dbSNP: rs1344706
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv
CUI: C0338614
Disease: Psychotic episodes
Psychotic episodes 		0.010 1.000 1 2015 2015
dbSNP: rs1344706
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv
CUI: C3160814
Disease: Cannabis use
Cannabis use 		0.010 1.000 1 2019 2019
dbSNP: rs1344706
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		0.010 1.000 1 2019 2019
dbSNP: rs1344706
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv
CUI: C0041696
Disease: Unipolar Depression
Unipolar Depression 		0.010 1.000 1 2018 2018
dbSNP: rs1344706
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv
CUI: C0006012
Disease: Borderline Personality Disorder
Borderline Personality Disorder 		0.010 1.000 1 2017 2017
dbSNP: rs1344706
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv
CUI: C0036363
Disease: Schizotypal Personality Disorder
Schizotypal Personality Disorder 		0.010 1.000 1 2011 2011
dbSNP: rs1344706
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv
CUI: C0085923
Disease: soft neurological signs
soft neurological signs 		0.010 1.000 1 2012 2012
dbSNP: rs1344706
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv
CUI: C0006287
Disease: Bronchopulmonary Dysplasia
Bronchopulmonary Dysplasia 		0.010 1.000 1 2017 2017
dbSNP: rs1344706
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.010 1.000 1 2018 2018
dbSNP: rs1344706
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv
CUI: C3887551
Disease: Memory dysfunction
Memory dysfunction 		0.010 1.000 1 2010 2010
dbSNP: rs1344706
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv
CUI: C0004936
Disease: Mental disorders
Mental disorders 		0.010 1.000 1 2019 2019
dbSNP: rs1344706
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.010 < 0.001 1 2019 2019