Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs3212227
IL12B
0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs243865
MMP2
0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs11536889
TLR4
0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11 27
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs10877887
LINC01465 ; MIRLET7I
0.701 0.440 12 62603400 non coding transcript exon variant T/C snv 0.42 18
rs767649
MIR155HG ; MIR155
0.695 0.480 21 25572410 intron variant T/A snv 7.5E-02 18
rs1333040
CDKN2B-AS1
0.732 0.280 9 22083405 intron variant C/G;T snv 15
rs2069718
IFNG ; IFNG-AS1
0.742 0.320 12 68156382 intron variant A/G;T snv 0.50 14
rs13293512 0.763 0.360 9 94167461 intron variant T/C snv 0.24 11
rs12413409
CNNM2
0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02 9
rs1746048 0.776 0.120 10 44280376 downstream gene variant C/T snv 0.25 8
rs2735971
MRPL23 ; H19
0.790 0.240 11 2000419 intron variant T/C snv 7
rs4705343
MIR143 ; CARMN
0.790 0.240 5 149428518 non coding transcript exon variant T/C snv 0.14 7
rs10757272
CDKN2B-AS1
0.851 0.160 9 22088261 intron variant C/T snv 0.41 6
rs496892
CDKN2B-AS1
0.827 0.160 9 22024352 intron variant C/T snv 0.40 6
rs1626340 0.827 0.120 9 99161090 intergenic variant G/A;T snv 5
rs6475606
CDKN2B-AS1
0.882 0.080 9 22081851 intron variant C/T snv 0.62 5
rs7660895
SLC2A9
0.882 0.200 4 9983821 intron variant A/G;T snv 5
rs4705342
MIR143 ; CARMN
0.851 0.160 5 149428408 non coding transcript exon variant T/C;G snv 4