FOXP1, forkhead box P1, 27086

N. diseases: 317; N. variants: 64
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: rs17008723
rs17008723 		0.925 0.040 3 71523984 intron variant T/G snv 0.15
CUI: C0042900
Disease: Vitiligo
Vitiligo 		Skin and Connective Tissue Diseases 0.700 1.000 1 2012 2012
dbSNP: rs34346645
rs34346645 		1.000 0.040 3 71508794 intron variant C/A snv 0.32
CUI: C0042900
Disease: Vitiligo
Vitiligo 		Skin and Connective Tissue Diseases 0.700 1.000 1 2016 2016