rs202247756, SUFU

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.
MENINGIOMA, FAMILIAL, SUSCEPTIBILITY TO
16 1.000 0.080 10 102550019 missense variant C/T snv 0.700 0
Meningioma
CUI: C0025286
Disease: Meningioma
43 1.000 0.080 10 102550019 missense variant C/T snv 0.010 1.000 1 2012 2012