rs1064794096, KLLN;PTEN

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 0.040 10 87864514 missense variant A/C;T snv 0.700 1.000 5 2007 2015
Glioma
CUI: C0017638
Disease: Glioma
353 1.000 0.040 10 87864514 missense variant A/C;T snv 0.700 0