rs1521, None

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.
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.882 0.320 6 31382927 upstream gene variant C/T snv 0.74 0.800 1.000 2 2011 2019
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.882 0.320 6 31382927 upstream gene variant C/T snv 0.74 0.700 1.000 1 2010 2010
Thyrotoxic periodic paralysis
CUI: C0268446
Disease: Thyrotoxic periodic paralysis
32 0.882 0.320 6 31382927 upstream gene variant C/T snv 0.74 0.700 1.000 1 2019 2019