rs12136280, LINC01136

N. diseases: 1
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.
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 1.000 0.120 1 203302802 intron variant G/T snv 0.35 0.010 1.000 1 2014 2014