rs189139, SH3BP2

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.
Huntington Disease
CUI: C0020179
Disease: Huntington Disease
115 0.925 0.160 4 2831000 intron variant C/T snv 0.26 0.700 1.000 1 2012 2012
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.925 0.160 4 2831000 intron variant C/T snv 0.26 0.700 1.000 1 2013 2013