rs4947296, 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.
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.851 0.440 6 31090401 intergenic variant T/A;C snv 0.810 0.667 3 2011 2019
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.851 0.440 6 31090401 intergenic variant T/A;C snv 0.800 1.000 2 2012 2013
Cardiomyopathy, Dilated
CUI: C0007193
Disease: Cardiomyopathy, Dilated
509 0.851 0.440 6 31090401 intergenic variant T/A;C snv 0.700 1.000 1 2014 2014
Thyrotoxic periodic paralysis
CUI: C0268446
Disease: Thyrotoxic periodic paralysis
32 0.851 0.440 6 31090401 intergenic variant T/A;C snv 0.700 1.000 1 2019 2019
Meniere Disease
CUI: C0025281
Disease: Meniere Disease
36 0.851 0.440 6 31090401 intergenic variant T/A;C snv 0.010 1.000 1 2017 2017