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: rs5753618
rs5753618 		0.790 0.080 22 31442532 intron variant C/T snv 0.20
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs5753618
rs5753618 		0.790 0.080 22 31442532 intron variant C/T snv 0.20
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs5753618
rs5753618 		0.790 0.080 22 31442532 intron variant C/T snv 0.20
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 1 2017 2017
dbSNP: rs5753618
rs5753618 		0.790 0.080 22 31442532 intron variant C/T snv 0.20
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs5753618
rs5753618 		0.790 0.080 22 31442532 intron variant C/T snv 0.20
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs5753618
rs5753618 		0.790 0.080 22 31442532 intron variant C/T snv 0.20
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 1 2017 2017
dbSNP: rs5753618
rs5753618 		0.790 0.080 22 31442532 intron variant C/T snv 0.20
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2017 2017
dbSNP: rs5753618
rs5753618 		0.790 0.080 22 31442532 intron variant C/T snv 0.20
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 1 2017 2017
dbSNP: rs5753618
rs5753618 		0.790 0.080 22 31442532 intron variant C/T snv 0.20
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs5753627
rs5753627 		22 31463873 synonymous variant A/G snv 0.10 6.8E-02
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs7289941
rs7289941 		1.000 0.040 22 31488419 intron variant T/A;C snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.010 1.000 1 2012 2012