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: rs13325108
rs13325108 		1.000 0.080 3 116671823 intron variant C/A;G snv
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		Neoplasms; Male Urogenital Diseases 0.700 1.000 1 2011 2011
dbSNP: rs1543175
rs1543175 		1.000 0.080 3 116668062 intron variant G/A snv 0.45
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		Neoplasms; Male Urogenital Diseases 0.700 1.000 1 2011 2011
dbSNP: rs17646258
rs17646258 		3 116319402 intron variant C/T snv 0.16
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2116308
rs2116308 		3 116387976 intron variant T/A;C;G snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs4378954
rs4378954 		0.790 0.080 3 115931601 intron variant T/C snv 0.83
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 1 2015 2015
dbSNP: rs4378954
rs4378954 		0.790 0.080 3 115931601 intron variant T/C snv 0.83
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 1 2015 2015
dbSNP: rs4378954
rs4378954 		0.790 0.080 3 115931601 intron variant T/C snv 0.83
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 1 2015 2015
dbSNP: rs4378954
rs4378954 		0.790 0.080 3 115931601 intron variant T/C snv 0.83
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2015 2015
dbSNP: rs4378954
rs4378954 		0.790 0.080 3 115931601 intron variant T/C snv 0.83
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2015 2015
dbSNP: rs4378954
rs4378954 		0.790 0.080 3 115931601 intron variant T/C snv 0.83
CUI: C0014170
Disease: Endometrial Neoplasms
Endometrial Neoplasms 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.700 1.000 1 2015 2015
dbSNP: rs4378954
rs4378954 		0.790 0.080 3 115931601 intron variant T/C snv 0.83
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2015 2015
dbSNP: rs4378954
rs4378954 		0.790 0.080 3 115931601 intron variant T/C snv 0.83
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2015 2015
dbSNP: rs4378954
rs4378954 		0.790 0.080 3 115931601 intron variant T/C snv 0.83
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2015 2015
dbSNP: rs4378954
rs4378954 		0.790 0.080 3 115931601 intron variant T/C snv 0.83
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2015 2015
dbSNP: rs9858874
rs9858874 		3 116782013 intron variant A/C snv 7.8E-03
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2011 2011