rs56250509, MLH1

N. diseases: 10
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 Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.790 0.160 3 37014530 missense variant T/C snv 2.0E-05 0.050 1.000 5 2002 2008
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.790 0.160 3 37014530 missense variant T/C snv 2.0E-05 0.030 1.000 3 2006 2008
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.790 0.160 3 37014530 missense variant T/C snv 2.0E-05 0.030 0.667 3 2007 2013
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.790 0.160 3 37014530 missense variant T/C snv 2.0E-05 0.030 0.667 3 2007 2013
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.790 0.160 3 37014530 missense variant T/C snv 2.0E-05 0.030 0.667 3 2007 2013
Squamous cell carcinoma of esophagus
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
329 0.790 0.160 3 37014530 missense variant T/C snv 2.0E-05 0.030 1.000 3 2008 2012
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.790 0.160 3 37014530 missense variant T/C snv 2.0E-05 0.010 1 2005 2005
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.790 0.160 3 37014530 missense variant T/C snv 2.0E-05 0.010 1.000 1 2014 2014
Methylenetetrahydrofolate reductase polymorphism
CUI: C2721734
Disease: Methylenetetrahydrofolate reductase polymorphism
7 0.790 0.160 3 37014530 missense variant T/C snv 2.0E-05 0.010 1.000 1 2013 2013
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.790 0.160 3 37014530 missense variant T/C snv 2.0E-05 0.010 1.000 1 2014 2014