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: rs4908760
rs4908760
RERE
1.000 0.040 1 8466082 intron variant G/A snv 0.68
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.800 1.000 2 2010 2012
dbSNP: rs301819
rs301819
RERE
0.882 0.120 1 8441726 intron variant A/G;T snv
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.700 1.000 1 2011 2011