Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4072037
MUC1
0.732 0.240 1 155192276 splice acceptor variant C/A;T snv 0.59 22
rs10754558
NLRP3
0.695 0.480 1 247448734 3 prime UTR variant G/C;T snv 20
rs1539019
NLRP3
0.882 0.240 1 247436999 intron variant A/C snv 0.63 6
rs1967017 0.882 0.160 1 145711421 upstream gene variant A/G snv 0.43 5
rs2990245
GBAP1
0.827 0.240 1 155227671 upstream gene variant C/G;T snv 5
rs4971100
TRIM46
0.925 0.120 1 155183255 intron variant G/A snv 0.39 5
rs11264341
TRIM46
0.925 0.120 1 155179017 intron variant C/T snv 0.40 4
rs4971059
TRIM46
0.851 0.200 1 155176305 intron variant G/A snv 0.34 4
rs9426886
TRIM46
0.851 0.200 1 155179278 intron variant A/T snv 0.40 4
rs10910845 0.925 0.120 1 145711946 upstream gene variant T/G snv 0.44 3
rs12123298
RNF115
0.925 0.120 1 145744615 3 prime UTR variant G/A;C snv 0.27 3
rs12129861
PDZK1
0.925 0.120 1 145709377 upstream gene variant C/T snv 0.43 3
rs12137901
NLRP3
0.882 0.200 1 247417907 intron variant T/C snv 0.26 3
rs12405132
RNF115
0.882 0.200 1 145790097 intron variant G/A snv 0.29 3
rs1471633 0.925 0.120 1 145711327 upstream gene variant T/G snv 0.43 3
rs4970988 0.925 0.120 1 150977586 upstream gene variant G/A snv 0.30 3
rs744877
CD160
0.882 0.200 1 145720709 intron variant C/A snv 0.47 3
rs7512998
NLRP3
0.882 0.200 1 247419919 intron variant C/T snv 0.83 3
rs7555340
ZMYM6
0.925 0.120 1 35015950 intron variant T/C snv 6.2E-03 3
rs9728619
PDZK1
0.925 0.120 1 145698627 intron variant A/G snv 0.51 3
rs1023945
CD160
0.925 0.120 1 145731972 intron variant G/A snv 0.55 2
rs10752826
POLR3C
0.925 0.120 1 145832321 intron variant C/G snv 0.37 2
rs11587821
POLR3C
0.925 0.120 1 145836072 intron variant C/A;T snv 2
rs11591191
RNF115
0.925 0.120 1 145759132 intron variant A/G snv 0.29 2
rs12402867
RNF115
0.925 0.120 1 145798852 intron variant C/T snv 0.29 2