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: rs710886
rs710886
0.763 0.160 8 127014615 intron variant C/T snv 0.37
CUI: C0014175
Disease: Endometriosis
Endometriosis
Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2020 2020
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: 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: 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: 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: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
Digestive System Diseases; Neoplasms 0.730 1.000 17 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: rs6983267
rs6983267
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
Malignant neoplasm of colon and/or rectum
0.100 0.933 15 2007 2019
dbSNP: rs6983267
rs6983267
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
Malignant neoplasm of large intestine
Digestive System Diseases; Neoplasms 0.700 1.000 14 2007 2019
dbSNP: rs6983267
rs6983267
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
0.700 1.000 14 2007 2019
dbSNP: rs6983267
rs6983267
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
0.700 1.000 14 2007 2019
dbSNP: rs6983267
rs6983267
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 14 2007 2019
dbSNP: rs6983267
rs6983267
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
0.700 1.000 14 2007 2019
dbSNP: rs6983267
rs6983267
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine
Digestive System Diseases; Neoplasms 0.700 1.000 14 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: 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: C0001430
Disease: Adenoma
Adenoma
Neoplasms 0.030 1.000 3 2008 2019
dbSNP: rs10086908
rs10086908
1.000 0.080 8 126999692 intron variant T/C snv 0.28
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
Neoplasms; Male Urogenital Diseases 0.700 1.000 2 2015 2019
dbSNP: rs10505477
rs10505477
0.658 0.400 8 127395198 intron variant A/G snv 0.40
CUI: C1302401
Disease: Adenoma of large intestine
Adenoma of large intestine
Digestive System Diseases; Neoplasms 0.020 1.000 2 2016 2019
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: rs16901946
rs16901946
0.827 0.160 8 127088680 non coding transcript exon variant A/G snv 1.7E-02
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
Digestive System Diseases; Neoplasms 0.020 1.000 2 2017 2019
dbSNP: rs16901946
rs16901946
0.827 0.160 8 127088680 non coding transcript exon variant A/G snv 1.7E-02
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
Digestive System Diseases; Neoplasms 0.020 1.000 2 2017 2019
dbSNP: rs7013278
rs7013278
0.776 0.080 8 127402647 intron variant T/C snv 0.59
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.710 1.000 2 2012 2019
dbSNP: rs1016343
rs1016343
0.807 0.240 8 127081052 non coding transcript exon variant C/T snv 0.20
Secondary malignant neoplasm of lymph node
Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2019 2019