rs179247, TSHR

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 0.882 0.160 14 80966202 intron variant A/G snv 0.40 0.770 1.000 8 2009 2017
Thyroid associated opthalmopathies
CUI: C0339143
Disease: Thyroid associated opthalmopathies
49 0.882 0.160 14 80966202 intron variant A/G snv 0.40 0.020 1.000 2 2014 2015
Disorder of eye
CUI: C0015397
Disease: Disorder of eye
14 0.882 0.160 14 80966202 intron variant A/G snv 0.40 0.010 1.000 1 2012 2012
Hashimoto Disease
CUI: C0677607
Disease: Hashimoto Disease
131 0.882 0.160 14 80966202 intron variant A/G snv 0.40 0.010 1.000 1 2017 2017
Thyroid Diseases
CUI: C0040128
Disease: Thyroid Diseases
26 0.882 0.160 14 80966202 intron variant A/G snv 0.40 0.010 1.000 1 2018 2018