Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs531564
LINC00599 ; MIR124-1
0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 27
rs2071559
KDR
0.667 0.680 4 55126199 upstream gene variant A/G snv 0.53 26
rs2249825
HMGB1
0.695 0.440 13 30463766 5 prime UTR variant G/A;C;T snv 23
rs187115
CD44
0.695 0.320 11 35154612 intron variant T/C snv 0.37 22
rs3748067
IL17A
0.672 0.320 6 52190541 3 prime UTR variant C/T snv 6.2E-02 21
rs10877887
LINC01465 ; MIRLET7I
0.701 0.440 12 62603400 non coding transcript exon variant T/C snv 0.42 18
rs1219648
FGFR2
0.716 0.320 10 121586676 intron variant A/G;T snv 17
rs1360485
HMGB1
0.742 0.320 13 30457747 3 prime UTR variant C/T snv 0.58 16
rs766914563
LOC112268426 ; CXCR4
0.732 0.320 2 136115082 synonymous variant C/T snv 7.0E-06 16
rs944289 0.742 0.200 14 36180040 upstream gene variant C/T snv 0.45 16
rs2302254
NME1-NME2 ; NME1
0.752 0.240 17 51153539 5 prime UTR variant C/T snv 0.22 15
rs965513
PTCSC2
0.742 0.200 9 97793827 intron variant A/G;T snv 15
rs11077
POLR1C ; XPO5
0.732 0.320 6 43523209 3 prime UTR variant T/G snv 0.47 14
rs13042395
SLC52A3
0.752 0.160 20 773867 intron variant C/T snv 5.9E-02 13
rs135745 0.763 0.200 22 38287631 downstream gene variant G/C snv 0.48 13
rs11886868
BCL11A
0.752 0.280 2 60493111 intron variant C/T snv 0.65 12
rs16949649
NME1 ; NME1-NME2
0.776 0.200 17 51152947 upstream gene variant T/C snv 0.39 12
rs931127
SIPA1 ; PCNX3
0.790 0.160 11 65637829 upstream gene variant G/A snv 0.49 12
rs11225395
MMP8
0.776 0.360 11 102725749 intron variant A/C;G snv 11
rs1143633
IL1B
0.752 0.280 2 112832890 intron variant C/G;T snv 11
rs116909374 0.776 0.120 14 36269155 regulatory region variant C/T snv 2.3E-02 11
rs13293512 0.763 0.360 9 94167461 intron variant T/C snv 0.24 11
rs3809865
THCAT158 ; ITGB3
0.790 0.240 17 47311220 3 prime UTR variant T/A;G snv 11
rs4671393
BCL11A
0.790 0.400 2 60493816 intron variant A/C;G snv 11
rs966423
DIRC3
0.776 0.200 2 217445617 intron variant C/G;T snv 11