rs623011, None

N. diseases: 5
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.
Thyrotoxic periodic paralysis
CUI: C0268446
Disease: Thyrotoxic periodic paralysis
32 0.827 0.320 17 70263305 intergenic variant A/G snv 0.74 0.710 1.000 3 2012 2019
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.827 0.320 17 70263305 intergenic variant A/G snv 0.74 0.700 1.000 1 2019 2019
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.827 0.320 17 70263305 intergenic variant A/G snv 0.74 0.010 1.000 1 2012 2012
Familial Periodic Paralysis
CUI: C0030443
Disease: Familial Periodic Paralysis
10 0.827 0.320 17 70263305 intergenic variant A/G snv 0.74 0.010 1.000 1 2012 2012
periodic paralysis (finding)
CUI: C1279412
Disease: periodic paralysis (finding)
11 0.827 0.320 17 70263305 intergenic variant A/G snv 0.74 0.010 1.000 1 2012 2012