Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1801275
IL4R
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 25
rs555743307
IL4R
0.695 0.440 16 27342243 missense variant G/A;T snv 3.6E-05; 2.9E-04 20
rs2069705
IFNG-AS1 ; IFNG
0.695 0.440 12 68161231 intron variant G/A;C snv 19
rs1805010
IL4R
0.752 0.400 16 27344882 missense variant A/C;G;T snv 0.45 12
rs743777
IL2RB
0.827 0.200 22 37155567 intron variant A/G snv 0.36 7
rs3218253
IL2RB
0.925 0.160 22 37148770 intron variant G/A snv 0.22 2