Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9617814 1.000 0.080 22 19622420 regulatory region variant A/G snv 0.22 1
rs2233406
NFKBIA
0.732 0.440 14 35405593 upstream gene variant G/A snv 0.26 12
rs2430561
IFNG ; IFNG-AS1
0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs12457893
BCL2
1.000 0.080 18 63258928 intron variant A/C snv 0.39 1
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs696
NFKBIA
0.708 0.520 14 35401887 3 prime UTR variant C/T snv 0.45 22