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: rs9841504
rs9841504 		0.827 0.120 3 114643917 intron variant C/G;T snv
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs9841504
rs9841504 		0.827 0.120 3 114643917 intron variant C/G;T snv
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs9841504
rs9841504 		0.827 0.120 3 114643917 intron variant C/G;T snv
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs9841504
rs9841504 		0.827 0.120 3 114643917 intron variant C/G;T snv
CUI: C0334037
Disease: Intestinal metaplasia
Intestinal metaplasia 		0.010 1.000 1 2017 2017
dbSNP: rs10511330
rs10511330 		0.776 0.080 3 114402172 intron variant T/C snv 0.22
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2018 2018
dbSNP: rs10511330
rs10511330 		0.776 0.080 3 114402172 intron variant T/C snv 0.22
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2018 2018
dbSNP: rs10511330
rs10511330 		0.776 0.080 3 114402172 intron variant T/C snv 0.22
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2018 2018
dbSNP: rs10511330
rs10511330 		0.776 0.080 3 114402172 intron variant T/C snv 0.22
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 1 2018 2018
dbSNP: rs10511330
rs10511330 		0.776 0.080 3 114402172 intron variant T/C snv 0.22
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2018 2018
dbSNP: rs10511330
rs10511330 		0.776 0.080 3 114402172 intron variant T/C snv 0.22
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 1 2018 2018
dbSNP: rs10511330
rs10511330 		0.776 0.080 3 114402172 intron variant T/C snv 0.22
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs10511330
rs10511330 		0.776 0.080 3 114402172 intron variant T/C snv 0.22
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2018 2018
dbSNP: rs10511330
rs10511330 		0.776 0.080 3 114402172 intron variant T/C snv 0.22
CUI: C1707439
Disease: Colorectal Mucinous Adenocarcinoma
Colorectal Mucinous Adenocarcinoma 		Neoplasms 0.700 1.000 1 2018 2018
dbSNP: rs10511330
rs10511330 		0.776 0.080 3 114402172 intron variant T/C snv 0.22
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 1 2018 2018
dbSNP: rs139459337
rs139459337 		0.882 0.040 3 114997018 intron variant C/T snv 4.7E-02
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs139459337
rs139459337 		0.882 0.040 3 114997018 intron variant C/T snv 4.7E-02
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs139459337
rs139459337 		0.882 0.040 3 114997018 intron variant C/T snv 4.7E-02
CUI: C0041696
Disease: Unipolar Depression
Unipolar Depression 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs1882289
rs1882289 		3 114742361 intron variant G/A snv 0.81
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2018 2018
dbSNP: rs1064795382
rs1064795382 		1.000 0.280 3 114339358 missense variant T/C snv
CUI: C0796121
Disease: Primrose syndrome
Primrose syndrome 		Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders; Otorhinolaryngologic Diseases; Behavior and Behavior Mechanisms 0.010 1.000 1 2019 2019
dbSNP: rs1533269
rs1533269 		3 114495764 intron variant C/A snv 0.43
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs17619973
rs17619973 		3 114698828 intron variant A/G snv 5.1E-02
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs17681451
rs17681451 		3 114680449 intron variant G/A snv 5.7E-02
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs2055981
rs2055981 		3 114485122 intron variant T/C snv 0.49
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs2399510
rs2399510 		3 114834387 intron variant C/A snv 0.82
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs6438208
rs6438208 		3 114451425 intron variant G/A snv 0.37
CUI: C0037369
Disease: Smoking
Smoking 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019