rs786202098, PMS2

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.
Hereditary Nonpolyposis Colorectal Neoplasms
875 7 6002638 splice acceptor variant T/C snv 0.700 1.000 3 2011 2016
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
6387 7 6002638 splice acceptor variant T/C snv 0.700 1.000 1 2016 2016