rs63751202, MLH1

N. diseases: 5
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 cancer, hereditary nonpolyposis, type 1
179 0.851 0.160 3 37048578 missense variant T/C;G snv 0.700 0
Hereditary Nonpolyposis Colorectal Cancer
1331 0.851 0.160 3 37048578 missense variant T/C;G snv 0.010 1.000 1 2013 2013
Lynch Syndrome
CUI: C4552100
Disease: Lynch Syndrome
65 0.851 0.160 3 37048578 missense variant T/C;G snv 0.010 1.000 1 2013 2013
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.851 0.160 3 37048578 missense variant T/C;G snv 0.010 1.000 1 2013 2013
MSI-high
CUI: C4523846
Disease: MSI-high
9 0.851 0.160 3 37048578 missense variant T/C;G snv 0.010 1.000 1 2013 2013