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: rs1847134
rs1847134
TYR ; LOC107984363
0.925 0.080 11 89272085 intron variant A/C snv 0.26
CUI: C0015396
Disease: Eye Color
Eye Color 		0.800 1.000 1 2010 2010
dbSNP: rs1847134
rs1847134
TYR ; LOC107984363
0.925 0.080 11 89272085 intron variant A/C snv 0.26
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.700 1.000 1 2010 2010