rs1801166, APC

N. diseases: 17
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 0.732 0.200 5 112839543 missense variant G/C snv 4.4E-03 5.6E-03 0.100 0.909 11 2000 2016
Malignant neoplasm of colon and/or rectum
502 0.732 0.200 5 112839543 missense variant G/C snv 4.4E-03 5.6E-03 0.080 0.875 8 2000 2016
Adenoma of large intestine
CUI: C1302401
Disease: Adenoma of large intestine
213 0.732 0.200 5 112839543 missense variant G/C snv 4.4E-03 5.6E-03 0.050 1.000 5 2000 2009
Adenomatous Polyposis Coli
CUI: C0032580
Disease: Adenomatous Polyposis Coli
237 0.732 0.200 5 112839543 missense variant G/C snv 4.4E-03 5.6E-03 0.040 1.000 4 2007 2015
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.732 0.200 5 112839543 missense variant G/C snv 4.4E-03 5.6E-03 0.040 0.750 4 2003 2009
Adenoma
CUI: C0001430
Disease: Adenoma
103 0.732 0.200 5 112839543 missense variant G/C snv 4.4E-03 5.6E-03 0.020 1.000 2 2002 2003
Adenomatous Polyps
CUI: C0206677
Disease: Adenomatous Polyps
20 0.732 0.200 5 112839543 missense variant G/C snv 4.4E-03 5.6E-03 0.020 1.000 2 2002 2003
Atrial Premature Complexes
CUI: C0033036
Disease: Atrial Premature Complexes
21 0.732 0.200 5 112839543 missense variant G/C snv 4.4E-03 5.6E-03 0.020 1.000 2 2007 2015
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.732 0.200 5 112839543 missense variant G/C snv 4.4E-03 5.6E-03 0.020 1.000 2 2003 2009
Carcinoma
CUI: C0007097
Disease: Carcinoma
103 0.732 0.200 5 112839543 missense variant G/C snv 4.4E-03 5.6E-03 0.010 1.000 1 2005 2005
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.732 0.200 5 112839543 missense variant G/C snv 4.4E-03 5.6E-03 0.010 1.000 1 1998 1998
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.732 0.200 5 112839543 missense variant G/C snv 4.4E-03 5.6E-03 0.010 1.000 1 2001 2001
FAMILIAL ADENOMATOUS POLYPOSIS, ATTENUATED (disorder)
7 0.732 0.200 5 112839543 missense variant G/C snv 4.4E-03 5.6E-03 0.010 1.000 1 2009 2009
Hyperplastic Polyp
CUI: C0333983
Disease: Hyperplastic Polyp
22 0.732 0.200 5 112839543 missense variant G/C snv 4.4E-03 5.6E-03 0.010 1.000 1 1998 1998
Medulloblastoma
CUI: C0025149
Disease: Medulloblastoma
115 0.732 0.200 5 112839543 missense variant G/C snv 4.4E-03 5.6E-03 0.010 1.000 1 2001 2001
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
257 0.732 0.200 5 112839543 missense variant G/C snv 4.4E-03 5.6E-03 0.010 1.000 1 2004 2004
Polyposis, Adenomatous Intestinal
CUI: C2713442
Disease: Polyposis, Adenomatous Intestinal
332 0.732 0.200 5 112839543 missense variant G/C snv 4.4E-03 5.6E-03 0.700 0