rs63750949, FBXO11;MSH6

N. diseases: 6
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 0.827 0.080 2 47806213 missense variant C/A;T snv 0.700 1.000 5 2002 2013
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.827 0.080 2 47806213 missense variant C/A;T snv 0.700 0
Adult Glioblastoma
CUI: C0278878
Disease: Adult Glioblastoma
98 0.827 0.080 2 47806213 missense variant C/A;T snv 0.010 1.000 1 2009 2009
Childhood Glioblastoma
CUI: C0280474
Disease: Childhood Glioblastoma
98 0.827 0.080 2 47806213 missense variant C/A;T snv 0.010 1.000 1 2009 2009
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
281 0.827 0.080 2 47806213 missense variant C/A;T snv 0.010 1.000 1 2009 2009
Glioblastoma Multiforme
CUI: C1621958
Disease: Glioblastoma Multiforme
186 0.827 0.080 2 47806213 missense variant C/A;T snv 0.010 1.000 1 2009 2009