rs529008617, MUTYH

N. diseases: 4
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 0.851 0.160 1 45331529 missense variant G/A snv 7.2E-05 2.8E-05 0.800 1.000 11 2002 2017
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
6385 0.851 0.160 1 45331529 missense variant G/A snv 7.2E-05 2.8E-05 0.700 1.000 18 2005 2017
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
100 0.851 0.160 1 45331529 missense variant G/A snv 7.2E-05 2.8E-05 0.700 1.000 4 2005 2010
B lymphoblastic leukemia lymphoma, no ICD-O subtype
CUI: C3472624
Disease: B lymphoblastic leukemia lymphoma, no ICD-O subtype
2 0.851 0.160 1 45331529 missense variant G/A snv 7.2E-05 2.8E-05 0.700 0