rs459552, APC

N. diseases: 13
Source: BEFREE ×
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.
Adenomatous Polyposis Coli
CUI: C0032580
Disease: Adenomatous Polyposis Coli
84 0.752 0.320 5 112841059 missense variant T/A;G snv 0.79 0.070 1.000 7 2001 2019
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1186 0.752 0.320 5 112841059 missense variant T/A;G snv 0.79 0.070 1.000 7 2003 2019
Malignant neoplasm of colon and/or rectum
502 0.752 0.320 5 112841059 missense variant T/A;G snv 0.79 0.040 1.000 4 2004 2019
Atrial Premature Complexes
CUI: C0033036
Disease: Atrial Premature Complexes
21 0.752 0.320 5 112841059 missense variant T/A;G snv 0.79 0.030 1.000 3 2003 2010
Adenoma
CUI: C0001430
Disease: Adenoma
103 0.752 0.320 5 112841059 missense variant T/A;G snv 0.79 0.010 1.000 1 2010 2010
Carcinoma, Ovarian Epithelial
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
321 0.752 0.320 5 112841059 missense variant T/A;G snv 0.79 0.010 1.000 1 2014 2014
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.752 0.320 5 112841059 missense variant T/A;G snv 0.79 0.010 1.000 1 2001 2001
Hypercholesterolemia
CUI: C0020443
Disease: Hypercholesterolemia
113 0.752 0.320 5 112841059 missense variant T/A;G snv 0.79 0.010 1.000 1 2007 2007
Malignant neoplasm of ovary
CUI: C1140680
Disease: Malignant neoplasm of ovary
246 0.752 0.320 5 112841059 missense variant T/A;G snv 0.79 0.010 1.000 1 2014 2014
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1441 0.752 0.320 5 112841059 missense variant T/A;G snv 0.79 0.010 1.000 1 2010 2010
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
289 0.752 0.320 5 112841059 missense variant T/A;G snv 0.79 0.010 1.000 1 2001 2001
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
229 0.752 0.320 5 112841059 missense variant T/A;G snv 0.79 0.010 1.000 1 2014 2014
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.752 0.320 5 112841059 missense variant T/A;G snv 0.79 0.010 1.000 1 2010 2010