rs6687758, None

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.
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.763 0.200 1 221991606 regulatory region variant A/G snv 0.20 0.840 1.000 8 2010 2019
Adenocarcinoma of large intestine
CUI: C1319315
Disease: Adenocarcinoma of large intestine
432 0.763 0.200 1 221991606 regulatory region variant A/G snv 0.20 0.700 1.000 5 2010 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
374 0.763 0.200 1 221991606 regulatory region variant A/G snv 0.20 0.700 1.000 5 2010 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
370 0.763 0.200 1 221991606 regulatory region variant A/G snv 0.20 0.700 1.000 5 2010 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
373 0.763 0.200 1 221991606 regulatory region variant A/G snv 0.20 0.700 1.000 5 2010 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
368 0.763 0.200 1 221991606 regulatory region variant A/G snv 0.20 0.700 1.000 5 2010 2019
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.763 0.200 1 221991606 regulatory region variant A/G snv 0.20 0.700 1.000 5 2010 2019
Malignant neoplasm of large intestine
375 0.763 0.200 1 221991606 regulatory region variant A/G snv 0.20 0.700 1.000 5 2010 2019
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.763 0.200 1 221991606 regulatory region variant A/G snv 0.20 0.700 1.000 5 2010 2019
Malignant neoplasm of colon and/or rectum
502 0.763 0.200 1 221991606 regulatory region variant A/G snv 0.20 0.020 1.000 2 2012 2018
Progressive supranuclear palsy
CUI: C0038868
Disease: Progressive supranuclear palsy
52 0.763 0.200 1 221991606 regulatory region variant A/G snv 0.20 0.810 1.000 2 2011 2018