rs9355610, LOC105378120

N. diseases: 3
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.
Primary biliary cirrhosis
CUI: C0008312
Disease: Primary biliary cirrhosis
667 0.882 0.200 6 166969587 downstream gene variant G/A;T snv 0.010 1.000 1 2017 2017
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.882 0.200 6 166969587 downstream gene variant G/A;T snv 0.850 1.000 6 2011 2018
Hyperthyroidism
CUI: C0020550
Disease: Hyperthyroidism
27 0.882 0.200 6 166969587 downstream gene variant G/A;T snv 0.010 1.000 1 2018 2018