rs6902119, FGFR1OP

N. diseases: 3
Source: ALL
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
249 0.882 0.160 6 167092303 intron variant T/C;G snv 0.700 1.000 2 2010 2012
Generalized vitiligo
CUI: C1304470
Disease: Generalized vitiligo
16 0.882 0.160 6 167092303 intron variant T/C;G snv 0.010 1.000 1 2010 2010
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.882 0.160 6 167092303 intron variant T/C;G snv 0.010 1.000 1 2015 2015