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: rs13076312
rs13076312
LPP
1.000 0.040 3 188371466 intron variant C/T snv 0.44
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.800 1.000 1 2010 2016
dbSNP: rs13076312
rs13076312
LPP
1.000 0.040 3 188371466 intron variant C/T snv 0.44
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 1.000 1 2013 2013