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: rs3789243
rs3789243 		0.776 0.120 7 87591570 intron variant A/G snv 0.50
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.030 1.000 3 2009 2013
dbSNP: rs1164376164
rs1164376164 		0.851 0.200 7 87601024 5 prime UTR variant A/G snv
CUI: C0001418
Disease: Adenocarcinoma
Adenocarcinoma 		Neoplasms 0.020 0.500 2 2006 2008
dbSNP: rs1202168
rs1202168 		1.000 0.080 7 87566646 intron variant G/A snv 0.39
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.020 1.000 2 2011 2012
dbSNP: rs1289543302
rs1289543302 		0.763 0.440 7 87536472 missense variant C/T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.020 1.000 2 2016 2017
dbSNP: rs3789243
rs3789243 		0.776 0.120 7 87591570 intron variant A/G snv 0.50
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.020 1.000 2 2009 2013
dbSNP: rs3789243
rs3789243 		0.776 0.120 7 87591570 intron variant A/G snv 0.50
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		0.020 0.500 2 2009 2013
dbSNP: rs3789243
rs3789243 		0.776 0.120 7 87591570 intron variant A/G snv 0.50
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.020 1.000 2 2009 2013
dbSNP: rs3789243
rs3789243 		0.776 0.120 7 87591570 intron variant A/G snv 0.50
CUI: C0001430
Disease: Adenoma
Adenoma 		Neoplasms 0.020 1.000 2 2009 2013
dbSNP: rs10234411
rs10234411 		1.000 0.040 7 87535576 intron variant T/A;C;G snv
CUI: C0014544
Disease: Epilepsy
Epilepsy 		Nervous System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs10264856
rs10264856 		7 87633265 intron variant G/A snv 0.16
CUI: C1314691
Disease: Age at menarche
Age at menarche 		Behavior and Behavior Mechanisms 0.700 1.000 1 2015 2015
dbSNP: rs1164376164
rs1164376164 		0.851 0.200 7 87601024 5 prime UTR variant A/G snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.010 1.000 1 2004 2004
dbSNP: rs1164376164
rs1164376164 		0.851 0.200 7 87601024 5 prime UTR variant A/G snv
CUI: C0023452
Disease: Childhood Acute Lymphoblastic Leukemia
Childhood Acute Lymphoblastic Leukemia 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2007 2007
dbSNP: rs1164376164
rs1164376164 		0.851 0.200 7 87601024 5 prime UTR variant A/G snv
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		Mental Disorders 0.010 1.000 1 2006 2006
dbSNP: rs1164376164
rs1164376164 		0.851 0.200 7 87601024 5 prime UTR variant A/G snv
CUI: C0079744
Disease: Diffuse Large B-Cell Lymphoma
Diffuse Large B-Cell Lymphoma 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2013 2013
dbSNP: rs1164376164
rs1164376164 		0.851 0.200 7 87601024 5 prime UTR variant A/G snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.010 1.000 1 2006 2006
dbSNP: rs1202184
rs1202184 		0.851 0.120 7 87584585 intron variant C/T snv 0.39
CUI: C0003467
Disease: Anxiety
Anxiety 		Behavior and Behavior Mechanisms 0.010 1.000 1 2011 2011
dbSNP: rs1202184
rs1202184 		0.851 0.120 7 87584585 intron variant C/T snv 0.39
CUI: C0003469
Disease: Anxiety Disorders
Anxiety Disorders 		Mental Disorders 0.010 1.000 1 2011 2011
dbSNP: rs1202184
rs1202184 		0.851 0.120 7 87584585 intron variant C/T snv 0.39
CUI: C0086132
Disease: Depressive Symptoms
Depressive Symptoms 		Behavior and Behavior Mechanisms 0.010 1.000 1 2011 2011
dbSNP: rs1202184
rs1202184 		0.851 0.120 7 87584585 intron variant C/T snv 0.39
CUI: C0011581
Disease: Depressive disorder
Depressive disorder 		Mental Disorders 0.010 1.000 1 2011 2011
dbSNP: rs1202184
rs1202184 		0.851 0.120 7 87584585 intron variant C/T snv 0.39
CUI: C0344315
Disease: Depressed mood
Depressed mood 		Behavior and Behavior Mechanisms 0.010 1.000 1 2011 2011
dbSNP: rs1202184
rs1202184 		0.851 0.120 7 87584585 intron variant C/T snv 0.39
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.010 1.000 1 2009 2009
dbSNP: rs1202184
rs1202184 		0.851 0.120 7 87584585 intron variant C/T snv 0.39
CUI: C0011570
Disease: Mental Depression
Mental Depression 		Behavior and Behavior Mechanisms 0.010 1.000 1 2011 2011
dbSNP: rs1202186
rs1202186 		1.000 0.040 7 87583942 intron variant C/T snv 0.69
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.010 1.000 1 2009 2009
dbSNP: rs12720066
rs12720066 		0.925 0.040 7 87540386 intron variant A/C snv 3.9E-02
CUI: C0023530
Disease: Leukopenia
Leukopenia 		Hemic and Lymphatic Diseases 0.010 1.000 1 2018 2018
dbSNP: rs12720066
rs12720066 		0.925 0.040 7 87540386 intron variant A/C snv 3.9E-02
CUI: C0027947
Disease: Neutropenia
Neutropenia 		Hemic and Lymphatic Diseases 0.010 1.000 1 2018 2018