Source: GWASCAT

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: rs145954018
rs145954018
1.000 0.040 6 32472545 intron variant GT/- delins
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2019 2019