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: rs6983267
rs6983267
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.900 0.945 55 2007 2019
dbSNP: rs10505477
rs10505477
0.658 0.400 8 127395198 intron variant A/G snv 0.40
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.890 0.938 16 2007 2019
dbSNP: rs7014346
rs7014346
0.732 0.240 8 127412547 intron variant A/G snv 0.63
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.830 0.889 9 2008 2019
dbSNP: rs6983267
rs6983267
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
Neoplasms; Male Urogenital Diseases 0.800 0.871 31 2007 2019
dbSNP: rs6983267
rs6983267
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
Neoplasms; Male Urogenital Diseases 0.800 0.857 28 2007 2017
dbSNP: rs13281615
rs13281615
0.716 0.360 8 127343372 intron variant A/G snv 0.43
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.800 0.864 22 2007 2017
dbSNP: rs16901979
rs16901979
0.724 0.480 8 127112671 intron variant C/A snv 0.16
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
Neoplasms; Male Urogenital Diseases 0.800 0.955 22 2007 2019
dbSNP: rs13281615
rs13281615
0.716 0.360 8 127343372 intron variant A/G snv 0.43
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.800 0.850 20 2007 2016
dbSNP: rs16901979
rs16901979
0.724 0.480 8 127112671 intron variant C/A snv 0.16
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
Neoplasms; Male Urogenital Diseases 0.800 0.950 20 2007 2018
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: rs6983561
rs6983561
0.925 0.080 8 127094635 intron variant A/C snv 0.17
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
Neoplasms; Male Urogenital Diseases 0.780 1.000 10 2008 2017
dbSNP: rs6983561
rs6983561
0.925 0.080 8 127094635 intron variant A/C snv 0.17
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
Neoplasms; Male Urogenital Diseases 0.780 1.000 9 2008 2017
dbSNP: rs6983267
rs6983267
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
Digestive System Diseases; Neoplasms 0.770 1.000 21 2007 2019
dbSNP: rs6983267
rs6983267
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
CUI: C1302401
Disease: Adenoma of large intestine
Adenoma of large intestine
Digestive System Diseases; Neoplasms 0.760 0.857 7 2010 2019
dbSNP: rs6983267
rs6983267
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
Digestive System Diseases; Neoplasms 0.730 1.000 17 2007 2019
dbSNP: rs1562430
rs1562430
0.807 0.160 8 127375606 intron variant T/C snv 0.41
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.730 1.000 5 2010 2015
dbSNP: rs1562430
rs1562430
0.807 0.160 8 127375606 intron variant T/C snv 0.41
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.730 1.000 5 2010 2015
dbSNP: rs16901966
rs16901966
0.925 0.080 8 127098007 intron variant A/G snv 0.13
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
Neoplasms; Male Urogenital Diseases 0.730 1.000 5 2008 2016
dbSNP: rs620861
rs620861
0.925 0.080 8 127323428 intron variant G/A snv 0.36
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
Neoplasms; Male Urogenital Diseases 0.730 0.750 4 2008 2017
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: rs7837328
rs7837328
0.882 0.120 8 127410882 intron variant A/G snv 0.52
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
Neoplasms; Male Urogenital Diseases 0.720 1.000 4 2008 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: rs16902094
rs16902094
0.882 0.160 8 127308101 intron variant A/G snv 0.15
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
Neoplasms; Male Urogenital Diseases 0.720 1.000 3 2009 2017