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: rs202110856
rs202110856 		0.790 0.080 5 96794169 intron variant -/C delins 2.1E-05
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2015 2015
dbSNP: rs202110856
rs202110856 		0.790 0.080 5 96794169 intron variant -/C delins 2.1E-05
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
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: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 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 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2015 2015
dbSNP: rs202110856
rs202110856 		0.790 0.080 5 96794169 intron variant -/C delins 2.1E-05
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2015 2015
dbSNP: rs202110856
rs202110856 		0.790 0.080 5 96794169 intron variant -/C delins 2.1E-05
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		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 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2015 2015
dbSNP: rs202110856
rs202110856 		0.790 0.080 5 96794169 intron variant -/C delins 2.1E-05
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2015 2015
dbSNP: rs2032890
rs2032890 		1.000 0.040 5 96785448 non coding transcript exon variant A/C;T snv
CUI: C0042165
Disease: Anterior uveitis
Anterior uveitis 		Eye Diseases 0.700 1.000 1 2015 2015
dbSNP: rs2549803
rs2549803 		0.827 0.120 5 96839226 intron variant C/T snv 0.27
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		Musculoskeletal Diseases 0.700 1.000 1 2016 2016
dbSNP: rs2549803
rs2549803 		0.827 0.120 5 96839226 intron variant C/T snv 0.27
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		Digestive System Diseases 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 		Digestive System Diseases 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 		Digestive System Diseases 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 		Skin and Connective Tissue Diseases 0.700 1.000 1 2016 2016
dbSNP: rs27033
rs27033 		5 96771195 intron variant T/A snv 0.52
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs27432
rs27432 		0.925 0.040 5 96783569 intron variant A/C;G snv
CUI: C0263361
Disease: Psoriasis vulgaris
Psoriasis vulgaris 		Skin and Connective Tissue Diseases 0.700 1.000 1 2015 2015
dbSNP: rs27710
rs27710 		1.000 0.040 5 96790494 intron variant A/G snv 0.62 0.63
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		Musculoskeletal Diseases 0.700 1.000 1 2011 2011
dbSNP: rs2910686
rs2910686 		0.827 0.120 5 96916885 intron variant T/C snv 0.42
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 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 		Digestive System Diseases 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 		Digestive System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs2927608
rs2927608 		5 96916728 intron variant G/A snv 0.42
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs34261036
rs34261036 		5 96895352 missense variant T/C;G snv 4.0E-06; 4.1E-03
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs35134
rs35134 		5 96823820 intron variant A/G snv 0.65
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.700 1.000 1 2019 2019
dbSNP: rs397964890
rs397964890 		5 96787817 intron variant -/AT;ATAT delins 0.63
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs39841
rs39841 		1.000 0.040 5 96784466 intron variant G/A;C snv
CUI: C0033860
Disease: Psoriasis
Psoriasis 		Skin and Connective Tissue Diseases 0.700 1.000 1 2015 2015