rs1412834, CDKN2B-AS1

N. diseases: 11
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.
Calcification of coronary artery
CUI: C1611184
Disease: Calcification of coronary artery
205 0.790 0.080 9 22110132 intron variant T/C snv 0.64 0.700 1.000 2 2011 2013
Adenocarcinoma of large intestine
CUI: C1319315
Disease: Adenocarcinoma of large intestine
432 0.790 0.080 9 22110132 intron variant T/C snv 0.64 0.700 1.000 1 2019 2019
Ankle brachial pressure index (observable entity)
40 0.790 0.080 9 22110132 intron variant T/C snv 0.64 0.700 1.000 1 2012 2012
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
374 0.790 0.080 9 22110132 intron variant T/C snv 0.64 0.700 1.000 1 2019 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
370 0.790 0.080 9 22110132 intron variant T/C snv 0.64 0.700 1.000 1 2019 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
373 0.790 0.080 9 22110132 intron variant T/C snv 0.64 0.700 1.000 1 2019 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
368 0.790 0.080 9 22110132 intron variant T/C snv 0.64 0.700 1.000 1 2019 2019
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.790 0.080 9 22110132 intron variant T/C snv 0.64 0.700 1.000 1 2019 2019
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.790 0.080 9 22110132 intron variant T/C snv 0.64 0.700 1.000 1 2019 2019
Malignant neoplasm of large intestine
375 0.790 0.080 9 22110132 intron variant T/C snv 0.64 0.700 1.000 1 2019 2019
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.790 0.080 9 22110132 intron variant T/C snv 0.64 0.700 1.000 1 2019 2019