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: rs2466035
rs2466035 		0.925 0.120 8 127198984 intron variant T/C snv 0.43
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.800 1.000 1 2013 2013
dbSNP: rs72725854
rs72725854 		0.925 0.080 8 127062570 intron variant A/G;T snv
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.710 1.000 1 2018 2018
dbSNP: rs10096351
rs10096351 		1.000 0.080 8 127359926 intron variant A/G snv 0.60
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 1 2017 2017
dbSNP: rs1016342
rs1016342 		1.000 0.080 8 127080210 non coding transcript exon variant C/G;T snv
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.700 1.000 1 2007 2007
dbSNP: rs1016343
rs1016343 		0.807 0.240 8 127081052 non coding transcript exon variant C/T snv 0.20
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases 0.700 1.000 1 2010 2010
dbSNP: rs1031588
rs1031588 		1.000 0.080 8 127081032 non coding transcript exon variant C/A snv 0.24
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.700 1.000 1 2007 2007
dbSNP: rs10505477
rs10505477 		0.658 0.400 8 127395198 intron variant A/G snv 0.40
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases 0.700 1.000 1 2010 2010
dbSNP: rs10505477
rs10505477 		0.658 0.400 8 127395198 intron variant A/G snv 0.40
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.700 1.000 1 2014 2014
dbSNP: rs10505477
rs10505477 		0.658 0.400 8 127395198 intron variant A/G snv 0.40
CUI: C0201544
Disease: Prostate specific antigen measurement
Prostate specific antigen measurement 		0.700 1.000 1 2017 2017
dbSNP: rs10505483
rs10505483 		0.925 0.080 8 127112950 intron variant C/T snv 0.16
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.700 1.000 1 2012 2012
dbSNP: rs10808555
rs10808555 		0.925 0.080 8 127397266 intron variant G/A snv 0.65
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2008 2008
dbSNP: rs10808556
rs10808556 		0.925 0.080 8 127400902 non coding transcript exon variant C/T snv 0.50
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		Neoplasms; Male Urogenital Diseases 0.700 1.000 1 2008 2008
dbSNP: rs12543663
rs12543663 		1.000 0.080 8 126912414 intron variant C/A;T snv
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		Neoplasms; Male Urogenital Diseases 0.700 1.000 1 2008 2008
dbSNP: rs12682344
rs12682344 		1.000 0.080 8 127094539 intron variant T/G snv 0.13
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.700 1.000 1 2014 2014
dbSNP: rs12682374
rs12682374 		0.790 0.080 8 127398703 intron variant C/A;G;T snv
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 1 2018 2018
dbSNP: rs12682374
rs12682374 		0.790 0.080 8 127398703 intron variant C/A;G;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2018 2018
dbSNP: rs12682374
rs12682374 		0.790 0.080 8 127398703 intron variant C/A;G;T snv
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 1 2018 2018
dbSNP: rs12682374
rs12682374 		0.790 0.080 8 127398703 intron variant C/A;G;T snv
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 1 2018 2018
dbSNP: rs12682374
rs12682374 		0.790 0.080 8 127398703 intron variant C/A;G;T snv
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: rs12682374
rs12682374 		0.790 0.080 8 127398703 intron variant C/A;G;T snv
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2018 2018
dbSNP: rs12682374
rs12682374 		0.790 0.080 8 127398703 intron variant C/A;G;T snv
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2018 2018
dbSNP: rs12682374
rs12682374 		0.790 0.080 8 127398703 intron variant C/A;G;T snv
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs12682374
rs12682374 		0.790 0.080 8 127398703 intron variant C/A;G;T snv
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2018 2018
dbSNP: rs13252298
rs13252298 		0.827 0.160 8 127082911 non coding transcript exon variant A/G snv 0.24
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		Neoplasms; Male Urogenital Diseases 0.700 1.000 1 2013 2013
dbSNP: rs13281615
rs13281615 		0.716 0.360 8 127343372 intron variant A/G snv 0.43
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases 0.700 1.000 1 2010 2010