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: rs1665650
rs1665650 		0.752 0.160 10 116727589 intron variant T/C snv 0.69
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.800 1.000 1 2013 2013
dbSNP: rs11197813
rs11197813 		10 116764422 intron variant A/C;G snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2018 2018
dbSNP: rs11592166
rs11592166 		10 116742544 5 prime UTR variant G/C snv 0.14
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs12259842
rs12259842 		1.000 0.040 10 116695732 intron variant C/G;T snv
CUI: C0025209
Disease: Melanosis
Melanosis 		Skin and Connective Tissue Diseases 0.700 1.000 1 2018 2018
dbSNP: rs1665650
rs1665650 		0.752 0.160 10 116727589 intron variant T/C snv 0.69
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 1 2013 2013
dbSNP: rs1665650
rs1665650 		0.752 0.160 10 116727589 intron variant T/C snv 0.69
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 1 2013 2013
dbSNP: rs1665650
rs1665650 		0.752 0.160 10 116727589 intron variant T/C snv 0.69
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2013 2013
dbSNP: rs1665650
rs1665650 		0.752 0.160 10 116727589 intron variant T/C snv 0.69
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2013 2013
dbSNP: rs1665650
rs1665650 		0.752 0.160 10 116727589 intron variant T/C snv 0.69
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2013 2013
dbSNP: rs1665650
rs1665650 		0.752 0.160 10 116727589 intron variant T/C snv 0.69
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 1 2013 2013
dbSNP: rs1665650
rs1665650 		0.752 0.160 10 116727589 intron variant T/C snv 0.69
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2013 2013
dbSNP: rs1665650
rs1665650 		0.752 0.160 10 116727589 intron variant T/C snv 0.69
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2013 2013
dbSNP: rs17095224
rs17095224 		10 116779732 intron variant A/G snv 1.8E-02
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs1665650
rs1665650 		0.752 0.160 10 116727589 intron variant T/C snv 0.69
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs1665650
rs1665650 		0.752 0.160 10 116727589 intron variant T/C snv 0.69
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs1665650
rs1665650 		0.752 0.160 10 116727589 intron variant T/C snv 0.69
CUI: C0595989
Disease: Carcinoma of larynx
Carcinoma of larynx 		Neoplasms; Respiratory Tract Diseases; Otorhinolaryngologic Diseases 0.010 1.000 1 2017 2017
dbSNP: rs740363
rs740363 		0.851 0.080 10 116816095 intron variant G/A snv 0.40
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.010 1.000 1 2007 2007
dbSNP: rs740363
rs740363 		0.851 0.080 10 116816095 intron variant G/A snv 0.40
CUI: C0018801
Disease: Heart failure
Heart failure 		Cardiovascular Diseases 0.010 1.000 1 2007 2007
dbSNP: rs740363
rs740363 		0.851 0.080 10 116816095 intron variant G/A snv 0.40
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2007 2007
dbSNP: rs740363
rs740363 		0.851 0.080 10 116816095 intron variant G/A snv 0.40
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.010 1.000 1 2007 2007
dbSNP: rs740363
rs740363 		0.851 0.080 10 116816095 intron variant G/A snv 0.40
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure 		Cardiovascular Diseases 0.010 1.000 1 2007 2007