rs1801155, APC

N. diseases: 31
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 Cancer
CUI: C1527249
Disease: Colorectal Cancer
955 0.657 0.393 5 112839514 missense variant T/A snp 2.0E-03; 8.0E-06 6.4E-04 0.100 0.720 25 1998 2006
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
539 0.657 0.393 5 112839514 missense variant T/A snp 2.0E-03; 8.0E-06 6.4E-04 0.100 0.708 24 1998 2006
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
240 0.657 0.393 5 112839514 missense variant T/A snp 2.0E-03; 8.0E-06 6.4E-04 0.070 0.714 7 1998 2004
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
135 0.657 0.393 5 112839514 missense variant T/A snp 2.0E-03; 8.0E-06 6.4E-04 0.070 0.714 7 1998 2004
Adenoma
CUI: C0001430
Disease: Adenoma
73 0.657 0.393 5 112839514 missense variant T/A snp 2.0E-03; 8.0E-06 6.4E-04 0.060 0.833 6 1999 2014
Adenomatous Polyposis Coli
CUI: C0032580
Disease: Adenomatous Polyposis Coli
31 0.657 0.393 5 112839514 missense variant T/A snp 2.0E-03; 8.0E-06 6.4E-04 0.050 1.000 5 1998 2016
Adenomatous Polyps
CUI: C0206677
Disease: Adenomatous Polyps
8 0.657 0.393 5 112839514 missense variant T/A snp 2.0E-03; 8.0E-06 6.4E-04 0.040 1.000 4 2000 2006
Malignant neoplasm of ovary
CUI: C1140680
Disease: Malignant neoplasm of ovary
244 0.657 0.393 5 112839514 missense variant T/A snp 2.0E-03; 8.0E-06 6.4E-04 0.040 0.750 4 1998 2000
Ovarian Carcinoma
CUI: C0029925
Disease: Ovarian Carcinoma
316 0.657 0.393 5 112839514 missense variant T/A snp 2.0E-03; 8.0E-06 6.4E-04 0.040 0.750 4 1998 2000
Atrial Premature Complexes
CUI: C0033036
Disease: Atrial Premature Complexes
9 0.657 0.393 5 112839514 missense variant T/A snp 2.0E-03; 8.0E-06 6.4E-04 0.030 1.000 3 1998 2016
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
226 0.657 0.393 5 112839514 missense variant T/A snp 2.0E-03; 8.0E-06 6.4E-04 0.030 1.000 3 1998 2005
Adenoma of large intestine
CUI: C1302401
Disease: Adenoma of large intestine
61 0.657 0.393 5 112839514 missense variant T/A snp 2.0E-03; 8.0E-06 6.4E-04 0.020 1.000 2 2005 2006
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
1839 0.657 0.393 5 112839514 missense variant T/A snp 2.0E-03; 8.0E-06 6.4E-04 0.020 1.000 2 1998 1999
Colonic Neoplasms
CUI: C0009375
Disease: Colonic Neoplasms
24 0.657 0.393 5 112839514 missense variant T/A snp 2.0E-03; 8.0E-06 6.4E-04 0.020 0.500 2 1999 2005
Colonic Polyps
CUI: C0009376
Disease: Colonic Polyps
2 0.657 0.393 5 112839514 missense variant T/A snp 2.0E-03; 8.0E-06 6.4E-04 0.020 0.500 2 2005 2005
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
451 0.657 0.393 5 112839514 missense variant T/A snp 2.0E-03; 8.0E-06 6.4E-04 0.020 0.500 2 1999 2001
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
1365 0.657 0.393 5 112839514 missense variant T/A snp 2.0E-03; 8.0E-06 6.4E-04 0.020 1.000 2 1998 1999
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
563 0.657 0.393 5 112839514 missense variant T/A snp 2.0E-03; 8.0E-06 6.4E-04 0.020 1.000 2 2003 2006
Polyp of large intestine
CUI: C0949059
Disease: Polyp of large intestine
15 0.657 0.393 5 112839514 missense variant T/A snp 2.0E-03; 8.0E-06 6.4E-04 0.020 1.000 2 1999 2000
polyps
CUI: C0032584
Disease: polyps
19 0.657 0.393 5 112839514 missense variant T/A snp 2.0E-03; 8.0E-06 6.4E-04 0.020 1.000 2 2001 2006
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
756 0.657 0.393 5 112839514 missense variant T/A snp 2.0E-03; 8.0E-06 6.4E-04 0.020 1.000 2 2003 2006
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
159 0.657 0.393 5 112839514 missense variant T/A snp 2.0E-03; 8.0E-06 6.4E-04 0.010 1.000 1 1998 1998
Epithelial ovarian cancer
CUI: C0677886
Disease: Epithelial ovarian cancer
197 0.657 0.393 5 112839514 missense variant T/A snp 2.0E-03; 8.0E-06 6.4E-04 0.010 1.000 1 1998 1998
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
223 0.657 0.393 5 112839514 missense variant T/A snp 2.0E-03; 8.0E-06 6.4E-04 0.010 1.000 1 1999 1999
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
60 0.657 0.393 5 112839514 missense variant T/A snp 2.0E-03; 8.0E-06 6.4E-04 0.010 1.000 1 1999 1999