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: rs812481
rs812481 		0.790 0.080 3 66392011 intron variant C/G snv 0.66
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 2 2015 2019
dbSNP: rs812481
rs812481 		0.790 0.080 3 66392011 intron variant C/G snv 0.66
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 2 2015 2019
dbSNP: rs812481
rs812481 		0.790 0.080 3 66392011 intron variant C/G snv 0.66
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 2 2015 2019
dbSNP: rs147372871
rs147372871 		1.000 0.080 3 66386050 missense variant G/A;T snv 2.9E-04; 4.0E-06
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 1.000 1 2018 2018
dbSNP: rs2306272
rs2306272 		1.000 0.080 3 66384219 missense variant T/C snv 0.31 0.25
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs2306272
rs2306272 		1.000 0.080 3 66384219 missense variant T/C snv 0.31 0.25
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs34080181
rs34080181 		1.000 0.080 3 66403767 intron variant G/A;C snv
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 1 2018 2018