rs786204931, PTEN

N. diseases: 3
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.
Hamartoma Syndrome, Multiple
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
139 0.925 0.120 10 87933126 missense variant C/G;T snv 0.700 1.000 8 1997 2012
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
6387 0.925 0.120 10 87933126 missense variant C/G;T snv 0.700 1.000 3 1997 2011
Endometrial Carcinoma
CUI: C0476089
Disease: Endometrial Carcinoma
326 0.925 0.120 10 87933126 missense variant C/G;T snv 0.700 0