rs1537372, CDKN2B-AS1

N. diseases: 14
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Adenocarcinoma of large intestine
CUI: C1319315
Disease: Adenocarcinoma of large intestine
432 0.752 0.120 9 22103184 intron variant G/A;T snv 0.700 1.000 1 2019 2019
Adenoma of large intestine
CUI: C1302401
Disease: Adenoma of large intestine
213 0.752 0.120 9 22103184 intron variant G/A;T snv 0.700 1.000 1 2019 2019
Calcification of coronary artery
CUI: C1611184
Disease: Calcification of coronary artery
205 0.752 0.120 9 22103184 intron variant G/A;T snv 0.700 1.000 1 2013 2013
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
374 0.752 0.120 9 22103184 intron variant G/A;T snv 0.700 1.000 1 2019 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
370 0.752 0.120 9 22103184 intron variant G/A;T snv 0.700 1.000 1 2019 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
373 0.752 0.120 9 22103184 intron variant G/A;T snv 0.700 1.000 1 2019 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
368 0.752 0.120 9 22103184 intron variant G/A;T snv 0.700 1.000 1 2019 2019
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.752 0.120 9 22103184 intron variant G/A;T snv 0.700 1.000 1 2019 2019
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.752 0.120 9 22103184 intron variant G/A;T snv 0.700 1.000 1 2019 2019
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.752 0.120 9 22103184 intron variant G/A;T snv 0.700 1.000 1 2013 2013
Malignant neoplasm of large intestine
CUI: C0346629
Disease: Malignant neoplasm of large intestine
375 0.752 0.120 9 22103184 intron variant G/A;T snv 0.700 1.000 1 2019 2019
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.752 0.120 9 22103184 intron variant G/A;T snv 0.700 1.000 1 2019 2019
Peripheral Arterial Diseases
CUI: C1704436
Disease: Peripheral Arterial Diseases
128 0.752 0.120 9 22103184 intron variant G/A;T snv 0.700 1.000 1 2019 2019
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.752 0.120 9 22103184 intron variant G/A;T snv 0.010 1.000 1 2016 2016