rs1265159, POU5F1

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.
Membranous glomerulonephritis
CUI: C0017665
Disease: Membranous glomerulonephritis
33 0.882 0.240 6 31172270 intron variant G/A snv 0.21 0.700 1.000 1 2011 2011
Myasthenia Gravis
CUI: C0026896
Disease: Myasthenia Gravis
93 0.882 0.240 6 31172270 intron variant G/A snv 0.21 0.700 1.000 1 2012 2012
Vitiligo
CUI: C0042900
Disease: Vitiligo
249 0.882 0.240 6 31172270 intron variant G/A snv 0.21 0.700 1.000 1 2010 2010