Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1265159
rs1265159
POU5F1
0.882 0.240 6 31172270 intron variant G/A snv 0.21
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.700 1.000 1 2010 2010
dbSNP: rs1265159
rs1265159
POU5F1
0.882 0.240 6 31172270 intron variant G/A snv 0.21
CUI: C0026896
Disease: Myasthenia Gravis
Myasthenia Gravis 		0.700 1.000 1 2012 2012