rs34612342, MUTYH

N. diseases: 32
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 Adenomatous Polyposis, Autosomal Recessive
112 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 0.800 1.000 23 2002 2017
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 0.800 1.000 17 2002 2019
MUTYH-Associate Polyposis
CUI: C3272841
Disease: MUTYH-Associate Polyposis
36 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 0.800 1.000 14 2005 2019
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 0.710 1.000 1 2015 2015
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
6387 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 0.700 1.000 8 2006 2017
Endometrial Carcinoma
CUI: C0476089
Disease: Endometrial Carcinoma
326 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 0.700 0
Malignant neoplasm of ovary
CUI: C1140680
Disease: Malignant neoplasm of ovary
315 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 0.700 0
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 0.700 0
Pilomatrixoma
CUI: C0206711
Disease: Pilomatrixoma
14 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 0.700 0
Skin Neoplasms
CUI: C0037286
Disease: Skin Neoplasms
9 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 0.700 0
Stomach Neoplasms
CUI: C0038356
Disease: Stomach Neoplasms
55 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 0.700 0
Malignant neoplasm of colon and/or rectum
502 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 0.050 1.000 5 2002 2011
Adenoma
CUI: C0001430
Disease: Adenoma
103 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 0.030 1.000 3 2010 2015
polyps
CUI: C0032584
Disease: polyps
18 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 0.030 1.000 3 2012 2019
Adenoma of large intestine
CUI: C1302401
Disease: Adenoma of large intestine
213 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 0.020 1.000 2 2002 2019
Adenomatous Polyposis Coli
CUI: C0032580
Disease: Adenomatous Polyposis Coli
237 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 0.020 1.000 2 2003 2007
Adenomatous Polyps
CUI: C0206677
Disease: Adenomatous Polyps
20 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 0.020 0.500 2 2004 2006
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 0.020 0.500 2 2009 2019
Head and Neck Carcinoma
CUI: C3887461
Disease: Head and Neck Carcinoma
118 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 0.020 1.000 2 2011 2015
Malignant Head and Neck Neoplasm
CUI: C0278996
Disease: Malignant Head and Neck Neoplasm
118 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 0.020 1.000 2 2011 2015
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 0.020 0.500 2 2009 2019
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 0.020 1.000 2 2017 2019
Childhood Acute Lymphoblastic Leukemia
261 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 0.010 1.000 1 2011 2011
Cholangiocarcinoma
CUI: C0206698
Disease: Cholangiocarcinoma
43 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 0.010 1.000 1 2006 2006
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 0.010 1.000 1 2015 2015