Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs4939827
rs4939827
0.708 0.160 18 48927093 intron variant T/A;C snv
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine
0.700 1.000 8 2007 2019
dbSNP: rs7229639
rs7229639
0.763 0.080 18 48924606 intron variant A/G snv 0.87
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine
0.700 1.000 5 2014 2019
dbSNP: rs11874392
rs11874392
0.763 0.080 18 48926786 intron variant A/T snv 0.50
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine
0.700 1.000 2 2016 2019
dbSNP: rs7226855
rs7226855
0.790 0.080 18 48927678 intron variant A/G;T snv
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine
0.700 1.000 2 2015 2019
dbSNP: rs12953717
rs12953717
0.724 0.240 18 48927559 intron variant C/T snv 0.36
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine
0.700 1.000 1 2017 2017
dbSNP: rs4939567
rs4939567
0.790 0.080 18 48925503 intron variant G/A snv 0.47
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine
0.700 1.000 1 2018 2018
dbSNP: rs6507874
rs6507874
0.790 0.080 18 48922435 intron variant T/C snv 0.54
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine
0.700 1.000 1 2018 2018
dbSNP: rs11874392
rs11874392
0.763 0.080 18 48926786 intron variant A/T snv 0.50
CUI: C1302401
Disease: Adenoma of large intestine
Adenoma of large intestine
0.700 1.000 1 2019 2019
dbSNP: rs7229639
rs7229639
0.763 0.080 18 48924606 intron variant A/G snv 0.87
CUI: C1302401
Disease: Adenoma of large intestine
Adenoma of large intestine
0.010 1.000 1 2016 2016
dbSNP: rs4939827
rs4939827
0.708 0.160 18 48927093 intron variant T/A;C snv
CUI: C0237123
Disease: Alcohol or Other Drugs use
Alcohol or Other Drugs use
0.010 1.000 1 2012 2012
dbSNP: rs9953366
rs9953366
1.000 0.080 18 48947822 intron variant T/A;C snv 0.72
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
0.700 1.000 2 2018 2018
dbSNP: rs2337107
rs2337107
0.882 0.120 18 48932953 intron variant C/T snv 0.52
CUI: C0431109
Disease: Choroid Plexus Carcinoma
Choroid Plexus Carcinoma
0.010 1.000 1 2012 2012
dbSNP: rs4464148
rs4464148
0.827 0.120 18 48932662 intron variant T/C snv 0.25
CUI: C0431109
Disease: Choroid Plexus Carcinoma
Choroid Plexus Carcinoma
0.010 1.000 1 2012 2012
dbSNP: rs12953717
rs12953717
0.724 0.240 18 48927559 intron variant C/T snv 0.36
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia
0.010 < 0.001 1 2008 2008
dbSNP: rs4939827
rs4939827
0.708 0.160 18 48927093 intron variant T/A;C snv
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.050 1.000 5 2008 2016
dbSNP: rs4464148
rs4464148
0.827 0.120 18 48932662 intron variant T/C snv 0.25
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.020 1.000 2 2009 2010
dbSNP: rs12953717
rs12953717
0.724 0.240 18 48927559 intron variant C/T snv 0.36
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 1.000 1 2010 2010
dbSNP: rs12953717
rs12953717
0.724 0.240 18 48927559 intron variant C/T snv 0.36
CUI: C0009375
Disease: Colonic Neoplasms
Colonic Neoplasms
0.010 1.000 1 2009 2009
dbSNP: rs4939827
rs4939827
0.708 0.160 18 48927093 intron variant T/A;C snv
CUI: C0009375
Disease: Colonic Neoplasms
Colonic Neoplasms
0.010 1.000 1 2009 2009
dbSNP: rs4939827
rs4939827
0.708 0.160 18 48927093 intron variant T/A;C snv
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
0.700 1.000 8 2007 2019
dbSNP: rs7229639
rs7229639
0.763 0.080 18 48924606 intron variant A/G snv 0.87
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
0.700 1.000 5 2014 2019
dbSNP: rs11874392
rs11874392
0.763 0.080 18 48926786 intron variant A/T snv 0.50
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
0.700 1.000 2 2016 2019
dbSNP: rs7226855
rs7226855
0.790 0.080 18 48927678 intron variant A/G;T snv
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
0.700 1.000 2 2015 2019
dbSNP: rs12953717
rs12953717
0.724 0.240 18 48927559 intron variant C/T snv 0.36
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
0.700 1.000 1 2017 2017
dbSNP: rs4939567
rs4939567
0.790 0.080 18 48925503 intron variant G/A snv 0.47
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
0.700 1.000 1 2018 2018