FGFR1OP, FGFR1 oncogene partner, 11116

N. diseases: 40; N. variants: 9
Disease: Vitiligo ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs6902119
rs6902119 		0.882 0.160 6 167092303 intron variant T/C;G snv
CUI: C0042900
Disease: Vitiligo
Vitiligo 		Skin and Connective Tissue Diseases 0.700 1.000 2 2010 2012