TYR, tyrosinase, 7299

N. diseases: 281; N. variants: 121
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: rs1393350
rs1393350 		0.851 0.160 11 89277878 intron variant G/A snv 0.17
CUI: C0042900
Disease: Vitiligo
Vitiligo 		Skin and Connective Tissue Diseases 0.800 1.000 3 2010 2012
dbSNP: rs1126809
rs1126809 		0.683 0.320 11 89284793 missense variant G/A snv 0.18 0.18
CUI: C0042900
Disease: Vitiligo
Vitiligo 		Skin and Connective Tissue Diseases 0.700 1.000 1 2016 2016
dbSNP: rs1847134
rs1847134 		0.925 0.080 11 89272085 intron variant A/C snv 0.26
CUI: C0042900
Disease: Vitiligo
Vitiligo 		Skin and Connective Tissue Diseases 0.700 1.000 1 2010 2010