rs1205829960, CTLA4

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.
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.925 0.160 2 203872753 missense variant C/G snv 7.0E-06 0.010 1.000 1 2008 2008
MYOTONIC DYSTROPHY 1
CUI: C3250443
Disease: MYOTONIC DYSTROPHY 1
14 0.925 0.160 2 203872753 missense variant C/G snv 7.0E-06 0.010 1.000 1 2004 2004