rs34612342, MUTYH

N. diseases: 11
Source: CLINVAR ×
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
CUI: C1837991
Disease: Colorectal Adenomatous Polyposis, Autosomal Recessive
98 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 0.800 1.000 23 2002 2017
MUTYH-Associate Polyposis
CUI: C3272841
Disease: MUTYH-Associate Polyposis
24 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 0.800 1.000 5 2005 2019
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
100 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 0.800 1.000 4 2002 2019
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
37 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 0.710 1.000 0 2015 2015
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
6385 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
28 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
20 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
72 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
2 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
47 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 0.700 0