rs3792783, TNIP1

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.
Myasthenia Gravis
CUI: C0026896
Disease: Myasthenia Gravis
93 0.882 0.280 5 151076171 intron variant A/G snv 0.25 0.700 1.000 1 2012 2012
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.882 0.280 5 151076171 intron variant A/G snv 0.25 0.700 1.000 1 2019 2019
Primary Sjögren's syndrome
CUI: C0151449
Disease: Primary Sjögren's syndrome
42 0.882 0.280 5 151076171 intron variant A/G snv 0.25 0.010 1.000 1 2013 2013