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.
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
322 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 0.010 1.000 1 2009 2009
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
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
Sebaceous Adenocarcinoma
CUI: C0206684
Disease: Sebaceous Adenocarcinoma
2 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 0.010 1.000 1 2014 2014
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
Squamous cell carcinoma of the head and neck
348 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 0.010 1.000 1 2011 2011
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