rs6902119, FGFR1OP

N. diseases: 1
Source: GWASDB ×
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Vitiligo
CUI: C0042900
Disease: Vitiligo
121 0.882 0.160 6 167092303 intron variant T/C;G snv 0.700 1.000 2 2010 2012