Disease: Vitiligo
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12153855
TNXB
0.776 0.320 6 32107027 intron variant T/C snv 0.11 10
rs12198173
TNXB
0.827 0.240 6 32059031 intron variant G/A snv 0.10 9
rs13199524
TNXB
0.807 0.240 6 32098988 intron variant C/T snv 8.4E-02 9