rs61747482, CEP128;TSHR

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 14 80955786 missense variant G/C snv 5.2E-03 5.0E-03 0.010 1 2002 2002