Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12733285
ADIPOR1
0.776 0.120 1 202952912 intron variant C/T snv 0.26 12
rs1342387
ADIPOR1
0.776 0.120 1 202945228 intron variant T/C snv 0.53 12
rs4803455
TGFB1
0.752 0.280 19 41345604 intron variant C/A snv 0.51 11
rs3753584
MTHFR ; CLCN6
0.827 0.080 1 11804529 5 prime UTR variant T/C snv 0.14 10
rs1061624
TNFRSF1B
0.776 0.320 1 12207208 3 prime UTR variant A/G snv 0.48 8
rs7747909
IL17A
0.790 0.320 6 52189451 3 prime UTR variant G/A snv 0.18 7
rs6854845 0.827 0.080 4 74821455 intergenic variant G/T snv 0.13 6
rs10484879
IL17A
0.827 0.160 6 52187159 intron variant G/A;T snv 5
rs2853668 0.882 0.080 5 1299910 upstream gene variant G/T snv 0.33 5
rs3775292
TLR3
0.851 0.080 4 186081871 non coding transcript exon variant C/G snv 0.82 5
rs9365723
SYNJ2
0.827 0.080 6 158014540 intron variant A/C;G snv 0.56 5
rs11721827
TLR3
0.851 0.200 4 186069983 intron variant A/C snv 0.12 4
rs17026425
IQCM
0.882 0.080 4 149751362 intron variant G/A snv 4.9E-02 4
rs1970764
PPP1R13L
0.851 0.120 19 45387615 intron variant T/C snv 0.27 4
rs3804513
IL17A
0.851 0.080 6 52188399 intron variant A/T snv 2.4E-02 4
rs11536898
TLR4
0.882 0.080 9 117717932 3 prime UTR variant C/A snv 0.14 3
rs2189517
RAD51B
0.882 0.080 14 68536271 intron variant A/G snv 0.49 3
rs2632159
LOC105375751 ; PCAT1
0.882 0.080 8 127021159 intron variant G/A;T snv 3
rs322351
DUSP1
0.925 0.160 5 172767870 intron variant C/T snv 0.37 3
rs10889675
IL23R
1.000 0.080 1 67256533 intron variant C/A snv 0.11 2
rs17268122
ABCC4
1.000 0.080 13 95192240 intron variant G/A;C;T snv 2
rs2073438
ALOX12 ; ALOX12-AS1
0.925 0.160 17 6996757 intron variant G/A snv 0.20 2
rs2269349
RPSA ; SNORA62
0.925 0.080 3 39411566 non coding transcript exon variant C/T snv 0.49 2
rs4596
GTF2H1
1.000 0.080 11 18366581 3 prime UTR variant G/C snv 0.41 2
rs7356
RPA2
1.000 0.080 1 27891589 3 prime UTR variant T/A;C snv 2