Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13194504 0.925 0.120 6 28662914 intergenic variant G/A snv 5.1E-02 2
rs11884476
PARD3B
2 205453869 intron variant C/G snv 0.11 1
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 1
rs4118325 1 107035210 intergenic variant G/A;T snv 1
rs6467710
DGKI
7 137519073 intron variant G/A;C snv 1