rs647161, C5orf66

N. diseases: 10
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.
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.776 0.080 5 135163402 intron variant C/A snv 0.63 0.820 1.000 6 2013 2019
Adenocarcinoma of large intestine
CUI: C1319315
Disease: Adenocarcinoma of large intestine
432 0.776 0.080 5 135163402 intron variant C/A snv 0.63 0.700 1.000 4 2013 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
374 0.776 0.080 5 135163402 intron variant C/A snv 0.63 0.700 1.000 4 2013 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
370 0.776 0.080 5 135163402 intron variant C/A snv 0.63 0.700 1.000 4 2013 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
373 0.776 0.080 5 135163402 intron variant C/A snv 0.63 0.700 1.000 4 2013 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
368 0.776 0.080 5 135163402 intron variant C/A snv 0.63 0.700 1.000 4 2013 2019
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.776 0.080 5 135163402 intron variant C/A snv 0.63 0.700 1.000 4 2013 2019
Malignant neoplasm of large intestine
375 0.776 0.080 5 135163402 intron variant C/A snv 0.63 0.700 1.000 4 2013 2019
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.776 0.080 5 135163402 intron variant C/A snv 0.63 0.700 1.000 4 2013 2019
Malignant neoplasm of colon and/or rectum
502 0.776 0.080 5 135163402 intron variant C/A snv 0.63 0.010 1.000 1 2018 2018