rs63750741, FBXO11;MSH6

N. diseases: 8
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.
Hereditary Nonpolyposis Colorectal Cancer
CUI: C1333990
Disease: Hereditary Nonpolyposis Colorectal Cancer
1331 0.827 0.200 2 47799329 missense variant T/C snv 1.2E-05 0.710 1.000 2 2004 2005
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.827 0.200 2 47799329 missense variant T/C snv 1.2E-05 0.700 1.000 12 1999 2012
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 5
CUI: C1833477
Disease: COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 5
78 0.827 0.200 2 47799329 missense variant T/C snv 1.2E-05 0.700 1.000 7 2004 2016
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
6387 0.827 0.200 2 47799329 missense variant T/C snv 1.2E-05 0.700 1.000 7 2004 2016
Endometrial Carcinoma
CUI: C0476089
Disease: Endometrial Carcinoma
326 0.827 0.200 2 47799329 missense variant T/C snv 1.2E-05 0.700 1.000 2 2000 2004
Hereditary Nonpolyposis Colorectal Neoplasms
CUI: C0009405
Disease: Hereditary Nonpolyposis Colorectal Neoplasms
875 0.827 0.200 2 47799329 missense variant T/C snv 1.2E-05 0.700 1.000 2 2005 2013
Lynch Syndrome
CUI: C4552100
Disease: Lynch Syndrome
65 0.827 0.200 2 47799329 missense variant T/C snv 1.2E-05 0.010 1.000 1 2005 2005
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.827 0.200 2 47799329 missense variant T/C snv 1.2E-05 0.010 1.000 1 2005 2005