rs1463038513, APC

N. diseases: 36
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.
Malignant neoplasm of ovary
CUI: C1140680
Disease: Malignant neoplasm of ovary
315 0.658 0.440 5 112839511 frameshift variant TAAA/- delins 0.020 1.000 2 1997 1998
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
757 0.658 0.440 5 112839511 frameshift variant TAAA/- delins 0.020 1.000 2 1997 1998
Polyp of large intestine
CUI: C0949059
Disease: Polyp of large intestine
32 0.658 0.440 5 112839511 frameshift variant TAAA/- delins 0.020 1.000 2 1999 2000
Colonic Polyps
CUI: C0009376
Disease: Colonic Polyps
8 0.658 0.440 5 112839511 frameshift variant TAAA/- delins 0.010 1.000 1 2005 2005
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.658 0.440 5 112839511 frameshift variant TAAA/- delins 0.010 1.000 1 1999 1999
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.658 0.440 5 112839511 frameshift variant TAAA/- delins 0.010 1.000 1 1999 1999
FAMILIAL ADENOMATOUS POLYPOSIS, ATTENUATED (disorder)
CUI: C2674616
Disease: FAMILIAL ADENOMATOUS POLYPOSIS, ATTENUATED (disorder)
7 0.658 0.440 5 112839511 frameshift variant TAAA/- delins 0.010 1.000 1 2012 2012
Hyperplastic Polyp
CUI: C0333983
Disease: Hyperplastic Polyp
22 0.658 0.440 5 112839511 frameshift variant TAAA/- delins 0.010 1.000 1 2000 2000
Lynch Syndrome
CUI: C4552100
Disease: Lynch Syndrome
65 0.658 0.440 5 112839511 frameshift variant TAAA/- delins 0.010 1.000 1 2017 2017
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.658 0.440 5 112839511 frameshift variant TAAA/- delins 0.010 1.000 1 1999 1999
Turcot syndrome (disorder)
CUI: C0265325
Disease: Turcot syndrome (disorder)
75 0.658 0.440 5 112839511 frameshift variant TAAA/- delins 0.010 1.000 1 1999 1999