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: rs3130284
rs3130284
AGPAT1
0.925 0.120 6 32172710 intron variant T/C snv 0.18
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.700 1.000 1 2010 2010
dbSNP: rs3134945
rs3134945
RNF5 ; AGPAT1 ; MIR6833
0.827 0.240 6 32178715 intron variant C/A snv 0.18
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.700 1.000 1 2010 2010
dbSNP: rs3134947
rs3134947
RNF5 ; AGPAT1
0.925 0.120 6 32177428 intron variant C/T snv 0.18
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.700 1.000 1 2010 2010