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: rs3806156
rs3806156
BTNL2 ; TSBP1-AS1
0.827 0.280 6 32405921 intron variant G/A;T snv
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.800 1.000 2 2010 2012
dbSNP: rs28362683
rs28362683
BTNL2 ; TSBP1-AS1
1.000 0.040 6 32405186 synonymous variant G/A snv 0.12 0.10
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.700 1.000 1 2011 2011