rs5912838, LOC107985690

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.
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.925 0.280 X 79241621 intergenic variant A/C snv 0.800 1.000 2 2013 2019
Thyrotoxic periodic paralysis
CUI: C0268446
Disease: Thyrotoxic periodic paralysis
32 0.925 0.280 X 79241621 intergenic variant A/C snv 0.700 1.000 1 2019 2019