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: rs679087
rs679087 		1.000 0.040 12 29764332 intron variant C/A;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 3 2014 2019
dbSNP: rs302321
rs302321 		1.000 0.040 12 29775455 intron variant C/A snv 0.24
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 2 2017 2019
dbSNP: rs2052678
rs2052678 		0.790 0.080 12 29680396 intron variant G/A snv 0.21
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2015 2015
dbSNP: rs2052678
rs2052678 		0.790 0.080 12 29680396 intron variant G/A snv 0.21
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2015 2015
dbSNP: rs2052678
rs2052678 		0.790 0.080 12 29680396 intron variant G/A snv 0.21
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2015 2015
dbSNP: rs2052678
rs2052678 		0.790 0.080 12 29680396 intron variant G/A snv 0.21
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: rs2052678
rs2052678 		0.790 0.080 12 29680396 intron variant G/A snv 0.21
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 1 2015 2015
dbSNP: rs2052678
rs2052678 		0.790 0.080 12 29680396 intron variant G/A snv 0.21
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2015 2015
dbSNP: rs2052678
rs2052678 		0.790 0.080 12 29680396 intron variant G/A snv 0.21
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 1 2015 2015
dbSNP: rs2052678
rs2052678 		0.790 0.080 12 29680396 intron variant G/A snv 0.21
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2015 2015
dbSNP: rs2052678
rs2052678 		0.790 0.080 12 29680396 intron variant G/A snv 0.21
CUI: C0014170
Disease: Endometrial Neoplasms
Endometrial Neoplasms 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.700 1.000 1 2015 2015
dbSNP: rs2052678
rs2052678 		0.790 0.080 12 29680396 intron variant G/A snv 0.21
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 1 2015 2015
dbSNP: rs78264913
rs78264913 		1.000 0.080 12 29733920 intron variant T/C snv 2.9E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 1 2019 2019