Source: GWASCAT ×
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
368 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 0.900 0.945 14 2007 2019
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
374 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 0.800 0.871 8 2007 2019
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
368 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 0.770 1.000 14 2007 2019
Adenoma of large intestine
CUI: C1302401
Disease: Adenoma of large intestine
114 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 0.760 0.857 1 2010 2019
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
368 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 0.730 1.000 14 2007 2019
Adenocarcinoma of large intestine
CUI: C1319315
Disease: Adenocarcinoma of large intestine
368 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 0.700 1.000 14 2007 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
368 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 0.700 1.000 14 2007 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
368 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 0.700 1.000 14 2007 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
368 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 0.700 1.000 14 2007 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
368 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 0.700 1.000 14 2007 2019
Malignant neoplasm of large intestine
368 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 0.700 1.000 14 2007 2019