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: rs10491487
rs10491487 		1.000 0.120 5 81027549 intron variant T/G snv 8.2E-02
CUI: C0011269
Disease: Dementia, Vascular
Dementia, Vascular 		Nervous System Diseases; Mental Disorders; Cardiovascular Diseases 0.700 1.000 1 2012 2012
dbSNP: rs13357015
rs13357015 		5 80967584 intron variant G/A snv 0.69
CUI: C0037369
Disease: Smoking
Smoking 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs138206701
rs138206701 		5 81110747 intron variant A/G snv 1.7E-02
CUI: C0013473
Disease: Eating Disorders
Eating Disorders 		Mental Disorders 0.700 1.000 1 2013 2013
dbSNP: rs138206701
rs138206701 		5 81110747 intron variant A/G snv 1.7E-02
CUI: C0029587
Disease: Other eating disorders
Other eating disorders 		Mental Disorders 0.700 1.000 1 2013 2013
dbSNP: rs17211233
rs17211233 		0.882 0.040 5 81072944 intron variant T/A;C snv
CUI: C0041696
Disease: Unipolar Depression
Unipolar Depression 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs17211233
rs17211233 		0.882 0.040 5 81072944 intron variant T/A;C snv
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs17211233
rs17211233 		0.882 0.040 5 81072944 intron variant T/A;C snv
CUI: C3546787
Disease: response to ketamine
response to ketamine 		0.700 1.000 1 2018 2018
dbSNP: rs17211233
rs17211233 		0.882 0.040 5 81072944 intron variant T/A;C snv
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs26906
rs26906 		1.000 0.120 5 81069068 intron variant T/C snv 0.86
CUI: C0011269
Disease: Dementia, Vascular
Dementia, Vascular 		Nervous System Diseases; Mental Disorders; Cardiovascular Diseases 0.700 1.000 1 2012 2012
dbSNP: rs1466151520
rs1466151520 		1.000 0.080 5 81094356 missense variant G/A snv 1.2E-05 2.8E-05
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		Neoplasms; Skin and Connective Tissue Diseases 0.700 0
dbSNP: rs779986744
rs779986744 		1.000 0.080 5 81042929 missense variant G/A;T snv 2.0E-05; 8.0E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.700 0
dbSNP: rs26907
rs26907 		0.882 0.240 5 81069496 intron variant G/A;T snv
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs26907
rs26907 		0.882 0.240 5 81069496 intron variant G/A;T snv
CUI: C0162309
Disease: Adrenoleukodystrophy
Adrenoleukodystrophy 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Endocrine System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs26907
rs26907 		0.882 0.240 5 81069496 intron variant G/A;T snv
CUI: C1623038
Disease: Cirrhosis
Cirrhosis 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2016 2016