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: rs12241008
rs12241008 		0.716 0.160 10 112520943 intron variant T/C snv 0.13
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.720 1.000 4 2014 2019
dbSNP: rs7086803
rs7086803 		0.763 0.160 10 112738717 intron variant G/A snv 0.20
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		Neoplasms; Respiratory Tract Diseases 0.720 1.000 3 2012 2018
dbSNP: rs7086803
rs7086803 		0.763 0.160 10 112738717 intron variant G/A snv 0.20
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		Neoplasms; Respiratory Tract Diseases 0.720 1.000 3 2012 2018
dbSNP: rs10506868
rs10506868 		0.716 0.160 10 112559621 intron variant C/T snv 3.1E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.720 1.000 2 2016 2018
dbSNP: rs7086803
rs7086803 		0.763 0.160 10 112738717 intron variant G/A snv 0.20
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma 		Neoplasms; Respiratory Tract Diseases 0.710 1.000 2 2015 2019
dbSNP: rs12241008
rs12241008 		0.716 0.160 10 112520943 intron variant T/C snv 0.13
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 3 2014 2019
dbSNP: rs12241008
rs12241008 		0.716 0.160 10 112520943 intron variant T/C snv 0.13
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 3 2014 2019
dbSNP: rs12241008
rs12241008 		0.716 0.160 10 112520943 intron variant T/C snv 0.13
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 3 2014 2019
dbSNP: rs12241008
rs12241008 		0.716 0.160 10 112520943 intron variant T/C snv 0.13
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 3 2014 2019
dbSNP: rs12241008
rs12241008 		0.716 0.160 10 112520943 intron variant T/C snv 0.13
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 3 2014 2019
dbSNP: rs12241008
rs12241008 		0.716 0.160 10 112520943 intron variant T/C snv 0.13
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		Digestive System Diseases; Neoplasms 0.700 1.000 3 2014 2019
dbSNP: rs12241008
rs12241008 		0.716 0.160 10 112520943 intron variant T/C snv 0.13
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		Digestive System Diseases; Neoplasms 0.700 1.000 3 2014 2019
dbSNP: rs12241008
rs12241008 		0.716 0.160 10 112520943 intron variant T/C snv 0.13
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 3 2014 2019
dbSNP: rs10506868
rs10506868 		0.716 0.160 10 112559621 intron variant C/T snv 3.1E-02
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 1 2016 2016
dbSNP: rs10506868
rs10506868 		0.716 0.160 10 112559621 intron variant C/T snv 3.1E-02
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs10506868
rs10506868 		0.716 0.160 10 112559621 intron variant C/T snv 3.1E-02
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs10506868
rs10506868 		0.716 0.160 10 112559621 intron variant C/T snv 3.1E-02
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 1 2016 2016
dbSNP: rs10506868
rs10506868 		0.716 0.160 10 112559621 intron variant C/T snv 3.1E-02
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 1 2016 2016
dbSNP: rs10506868
rs10506868 		0.716 0.160 10 112559621 intron variant C/T snv 3.1E-02
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2016 2016
dbSNP: rs10506868
rs10506868 		0.716 0.160 10 112559621 intron variant C/T snv 3.1E-02
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs10506868
rs10506868 		0.716 0.160 10 112559621 intron variant C/T snv 3.1E-02
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs10787453
rs10787453 		10 112624298 intron variant G/A snv 0.68
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs11599775
rs11599775 		1.000 0.040 10 112699938 intron variant G/A snv 0.27
CUI: C0017638
Disease: Glioma
Glioma 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs11599775
rs11599775 		1.000 0.040 10 112699938 intron variant G/A snv 0.27
CUI: C0085136
Disease: Central Nervous System Neoplasms
Central Nervous System Neoplasms 		Neoplasms; Nervous System Diseases 0.700 1.000 1 2017 2017
dbSNP: rs12246635
rs12246635 		0.776 0.080 10 112528860 intron variant T/C snv 0.13
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2019 2019