rs4936742, UBASH3B

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.
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.925 0.200 11 122770378 intron variant T/C snv 0.64 0.010 1.000 1 2019 2019
Uveitis, Posterior
CUI: C0042167
Disease: Uveitis, Posterior
5 0.925 0.200 11 122770378 intron variant T/C snv 0.64 0.010 1.000 1 2019 2019