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: rs1456315
rs1456315 		0.790 0.200 8 127091692 non coding transcript exon variant T/A;C snv
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		Neoplasms; Male Urogenital Diseases 0.720 1.000 6 2010 2014
dbSNP: rs1456315
rs1456315 		0.790 0.200 8 127091692 non coding transcript exon variant T/A;C snv
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.720 1.000 4 2010 2014
dbSNP: rs13254738
rs13254738 		0.807 0.160 8 127092098 non coding transcript exon variant C/A;T snv
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.720 0.667 3 2008 2012
dbSNP: rs13254738
rs13254738 		0.807 0.160 8 127092098 non coding transcript exon variant C/A;T snv
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		Neoplasms; Male Urogenital Diseases 0.720 0.667 3 2008 2012
dbSNP: rs188140481
rs188140481 		0.925 0.080 8 127179427 non coding transcript exon variant T/A;C snv
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.720 1.000 3 2012 2015
dbSNP: rs445114
rs445114 		0.882 0.160 8 127310936 intron variant T/A;C snv
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		Neoplasms; Male Urogenital Diseases 0.700 1.000 3 2009 2013
dbSNP: rs13256367
rs13256367 		8 127322655 intron variant A/C;T snv
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 2 2018 2019
dbSNP: rs1456315
rs1456315 		0.790 0.200 8 127091692 non coding transcript exon variant T/A;C snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.020 1.000 2 2013 2019
dbSNP: rs188140481
rs188140481 		0.925 0.080 8 127179427 non coding transcript exon variant T/A;C snv
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		Neoplasms; Male Urogenital Diseases 0.020 1.000 2 2015 2015
dbSNP: rs445114
rs445114 		0.882 0.160 8 127310936 intron variant T/A;C snv
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.700 1.000 2 2009 2011
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: 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: 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: rs13254738
rs13254738 		0.807 0.160 8 127092098 non coding transcript exon variant C/A;T snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.010 < 0.001 1 2008 2008
dbSNP: rs13254738
rs13254738 		0.807 0.160 8 127092098 non coding transcript exon variant C/A;T snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		Neoplasms; Skin and Connective Tissue Diseases 0.010 < 0.001 1 2008 2008
dbSNP: rs13254738
rs13254738 		0.807 0.160 8 127092098 non coding transcript exon variant C/A;T snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.010 < 0.001 1 2008 2008
dbSNP: rs13254738
rs13254738 		0.807 0.160 8 127092098 non coding transcript exon variant C/A;T snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.010 < 0.001 1 2008 2008