Source: CURATED ×
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 3
rs3131093 0.925 0.160 6 28869660 intergenic variant C/T snv 7.1E-02 3
rs1799864
CCR2
0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 2
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 2
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv 2
rs4118325 1 107035210 intergenic variant G/A;T snv 1
rs6467710
DGKI
7 137519073 intron variant G/A;C snv 1
rs11884476
PARD3B
2 205453869 intron variant C/G snv 0.11 1