rs397514684, MLH1

N. diseases: 2
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.
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
6387 1.000 0.160 3 37000965 missense variant T/C;G snv 0.700 1.000 1 2013 2013
Turcot syndrome (disorder)
CUI: C0265325
Disease: Turcot syndrome (disorder)
75 1.000 0.160 3 37000965 missense variant T/C;G snv 0.700 0