rs1114167857, MSH2

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 0.080 2 47476442 missense variant T/C snv 0.700 1.000 2 2010 2017
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 1.000 0.080 2 47476442 missense variant T/C snv 0.010 1.000 1 2010 2010