rs10786691, SUFU

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.
Congenital cerebral hernia
CUI: C0014065
Disease: Congenital cerebral hernia
6 0.925 0.160 10 102604895 intron variant G/A;T snv 0.010 1.000 1 2014 2014
Encephalocele
CUI: C4551722
Disease: Encephalocele
7 0.925 0.160 10 102604895 intron variant G/A;T snv 0.010 1.000 1 2014 2014
Neural Tube Defects
CUI: C0027794
Disease: Neural Tube Defects
122 0.925 0.160 10 102604895 intron variant G/A;T snv 0.010 1.000 1 2014 2014