rs17137412, UMAD1

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.
Stevens-Johnson Syndrome
CUI: C0038325
Disease: Stevens-Johnson Syndrome
16 0.925 0.160 7 7761056 intron variant T/G snv 0.17 0.700 1.000 1 2012 2012
Toxic Epidermal Necrolysis
CUI: C0014518
Disease: Toxic Epidermal Necrolysis
29 0.925 0.160 7 7761056 intron variant T/G snv 0.17 0.700 1.000 1 2012 2012