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: rs12701020
rs12701020 		0.925 0.040 7 30655345 intron variant C/T snv 0.12
CUI: C0006012
Disease: Borderline Personality Disorder
Borderline Personality Disorder 		Mental Disorders 0.010 1.000 1 2016 2016
dbSNP: rs12701020
rs12701020 		0.925 0.040 7 30655345 intron variant C/T snv 0.12
CUI: C0013146
Disease: Drug abuse
Drug abuse 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2016 2016
dbSNP: rs12701020
rs12701020 		0.925 0.040 7 30655345 intron variant C/T snv 0.12
CUI: C4296683
Disease: Emotional neglect
Emotional neglect 		0.010 1.000 1 2016 2016
dbSNP: rs2267715
rs2267715 		1.000 0.040 7 30676471 intron variant G/A;C snv
CUI: C0038436
Disease: Post-Traumatic Stress Disorder
Post-Traumatic Stress Disorder 		Mental Disorders 0.010 1.000 1 2020 2020
dbSNP: rs2267716
rs2267716 		0.851 0.120 7 30677027 intron variant T/A;C snv
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic 		Digestive System Diseases; Infections 0.010 1.000 1 2010 2010
dbSNP: rs2267716
rs2267716 		0.851 0.120 7 30677027 intron variant T/A;C snv
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2010 2010
dbSNP: rs2267716
rs2267716 		0.851 0.120 7 30677027 intron variant T/A;C snv
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		Digestive System Diseases; Infections 0.010 1.000 1 2010 2010
dbSNP: rs2267716
rs2267716 		0.851 0.120 7 30677027 intron variant T/A;C snv
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.010 1.000 1 2010 2010
dbSNP: rs2267717
rs2267717 		1.000 0.040 7 30677427 intron variant G/A snv 0.17
CUI: C1842981
Disease: NEUROTICISM
NEUROTICISM 		Behavior and Behavior Mechanisms 0.010 < 0.001 1 2006 2006
dbSNP: rs255105
rs255105 		1.000 0.080 7 30692491 intron variant T/C snv 0.50
CUI: C0019337
Disease: Heroin Dependence
Heroin Dependence 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2018 2018
dbSNP: rs3779250
rs3779250 		0.925 0.080 7 30654644 intron variant C/T snv 0.48
CUI: C0022104
Disease: Irritable Bowel Syndrome
Irritable Bowel Syndrome 		Digestive System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs3779250
rs3779250 		0.925 0.080 7 30654644 intron variant C/T snv 0.48
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.010 1.000 1 2012 2012
dbSNP: rs4722999
rs4722999 		0.851 0.080 7 30654159 intron variant C/T snv 0.67
CUI: C4296683
Disease: Emotional neglect
Emotional neglect 		0.010 1.000 1 2016 2016
dbSNP: rs4722999
rs4722999 		0.851 0.080 7 30654159 intron variant C/T snv 0.67
CUI: C0022104
Disease: Irritable Bowel Syndrome
Irritable Bowel Syndrome 		Digestive System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs4722999
rs4722999 		0.851 0.080 7 30654159 intron variant C/T snv 0.67
CUI: C0006012
Disease: Borderline Personality Disorder
Borderline Personality Disorder 		Mental Disorders 0.010 1.000 1 2016 2016
dbSNP: rs4722999
rs4722999 		0.851 0.080 7 30654159 intron variant C/T snv 0.67
CUI: C0013146
Disease: Drug abuse
Drug abuse 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2016 2016
dbSNP: rs4722999
rs4722999 		0.851 0.080 7 30654159 intron variant C/T snv 0.67
CUI: C0030319
Disease: Panic Disorder
Panic Disorder 		Mental Disorders 0.010 1.000 1 2012 2012
dbSNP: rs7793837
rs7793837 		1.000 0.080 7 30687161 intron variant A/C;T snv
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2008 2008