Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2230926
TNFAIP3
0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 27
rs5029939
TNFAIP3
0.701 0.440 6 137874586 intron variant C/G snv 0.13 19
rs77191406
TNFAIP3
0.790 0.280 6 137881704 3 prime UTR variant C/T snv 7.2E-04 12
rs582757
TNFAIP3
0.776 0.320 6 137876687 intron variant C/T snv 0.70 8
rs610604
TNFAIP3
0.827 0.240 6 137878280 intron variant G/T snv 0.58 5
rs5029937
TNFAIP3
0.882 0.160 6 137874014 intron variant G/T snv 0.13 4
rs5029924
TNFAIP3 ; WAKMAR2
0.851 0.200 6 137866361 intron variant C/T snv 0.13 4
rs1423560438
TNFAIP3
0.882 0.080 6 137875748 stop gained C/T snv 3
rs143002189
TNFAIP3
1.000 0.120 6 137881310 missense variant G/A snv 4.3E-04 4.4E-04 3
rs661561
TNFAIP3
0.882 0.200 6 137876194 intron variant A/C snv 0.62 0.50 3
rs583522
WAKMAR2 ; TNFAIP3
0.925 0.080 6 137868747 intron variant C/A;T snv 3
rs2307859
TNFAIP3
0.925 0.120 6 137874825 intron variant CCT/- delins 2
rs5029941
TNFAIP3
1.000 0.080 6 137874923 missense variant C/T snv 1.2E-03 5.6E-03 2
rs5029949
TNFAIP3
0.925 0.120 6 137876369 intron variant A/G snv 8.1E-02 2
rs146534657
TNFAIP3
1.000 0.120 6 137874854 missense variant A/G snv 1.4E-02 6.0E-03 1
rs368859219
TNFAIP3
1.000 0.040 6 137881228 missense variant G/A;T snv 7.4E-05; 8.2E-06 1
rs598493
TNFAIP3
1.000 0.120 6 137874265 intron variant T/C snv 0.71 1
rs643177
TNFAIP3
1.000 0.040 6 137874556 intron variant T/C snv 0.70 1
rs719149
TNFAIP3
1.000 0.120 6 137871608 intron variant G/A snv 0.19 1
rs719150
TNFAIP3
6 137871624 intron variant A/G snv 0.20 1
rs864321625
TNFAIP3
1.000 6 137876041 stop gained T/A snv 1
rs864321626
TNFAIP3
1.000 6 137877081 stop gained C/T snv 1
rs864321682
TNFAIP3
1.000 6 137876030 frameshift variant T/- delins 1
rs864321683
TNFAIP3
1.000 6 137879251 frameshift variant G/- delins 1
rs864321684
TNFAIP3
1.000 6 137877188 stop gained C/G snv 1