Source: GWASCAT

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: rs202110856
rs202110856
0.790 0.080 5 96794169 intron variant -/C delins 2.1E-05
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
0.700 1.000 1 2015 2015
dbSNP: rs202110856
rs202110856
0.790 0.080 5 96794169 intron variant -/C delins 2.1E-05
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.700 1.000 1 2015 2015
dbSNP: rs202110856
rs202110856
0.790 0.080 5 96794169 intron variant -/C delins 2.1E-05
Malignant neoplasm of large intestine
0.700 1.000 1 2015 2015
dbSNP: rs202110856
rs202110856
0.790 0.080 5 96794169 intron variant -/C delins 2.1E-05
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
0.700 1.000 1 2015 2015
dbSNP: rs202110856
rs202110856
0.790 0.080 5 96794169 intron variant -/C delins 2.1E-05
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
0.700 1.000 1 2015 2015
dbSNP: rs202110856
rs202110856
0.790 0.080 5 96794169 intron variant -/C delins 2.1E-05
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine
0.700 1.000 1 2015 2015
dbSNP: rs202110856
rs202110856
0.790 0.080 5 96794169 intron variant -/C delins 2.1E-05
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 1 2015 2015
dbSNP: rs202110856
rs202110856
0.790 0.080 5 96794169 intron variant -/C delins 2.1E-05
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
0.700 1.000 1 2015 2015
dbSNP: rs202110856
rs202110856
0.790 0.080 5 96794169 intron variant -/C delins 2.1E-05
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 1 2015 2015
dbSNP: rs2910686
rs2910686
0.827 0.120 5 96916885 intron variant T/C snv 0.42
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.700 1.000 2 2012 2016
dbSNP: rs2910686
rs2910686
0.827 0.120 5 96916885 intron variant T/C snv 0.42
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.700 1.000 2 2013 2016
dbSNP: rs2549803
rs2549803
0.827 0.120 5 96839226 intron variant C/T snv 0.27
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing
0.700 1.000 1 2016 2016
dbSNP: rs2549803
rs2549803
0.827 0.120 5 96839226 intron variant C/T snv 0.27
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.700 1.000 1 2016 2016
dbSNP: rs2549803
rs2549803
0.827 0.120 5 96839226 intron variant C/T snv 0.27
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.700 1.000 1 2016 2016
dbSNP: rs2549803
rs2549803
0.827 0.120 5 96839226 intron variant C/T snv 0.27
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2016 2016
dbSNP: rs2549803
rs2549803
0.827 0.120 5 96839226 intron variant C/T snv 0.27
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.700 1.000 1 2016 2016
dbSNP: rs2910686
rs2910686
0.827 0.120 5 96916885 intron variant T/C snv 0.42
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing
0.700 1.000 1 2016 2016
dbSNP: rs2910686
rs2910686
0.827 0.120 5 96916885 intron variant T/C snv 0.42
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.700 1.000 1 2016 2016
dbSNP: rs2910686
rs2910686
0.827 0.120 5 96916885 intron variant T/C snv 0.42
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2016 2016
dbSNP: rs469758
rs469758
0.827 0.120 5 96786011 intron variant C/T snv 0.62 0.63
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.700 1.000 1 2016 2016
dbSNP: rs469758
rs469758
0.827 0.120 5 96786011 intron variant C/T snv 0.62 0.63
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2016 2016
dbSNP: rs469758
rs469758
0.827 0.120 5 96786011 intron variant C/T snv 0.62 0.63
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.700 1.000 1 2016 2016
dbSNP: rs469758
rs469758
0.827 0.120 5 96786011 intron variant C/T snv 0.62 0.63
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing
0.700 1.000 1 2016 2016
dbSNP: rs469758
rs469758
0.827 0.120 5 96786011 intron variant C/T snv 0.62 0.63
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.700 1.000 1 2016 2016
dbSNP: rs27524
rs27524
0.851 0.160 5 96766240 intron variant A/G snv 0.61
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.800 1.000 2 2010 2015