Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs374039502
TNFSF13B
0.925 0.160 13 108308037 3 prime UTR variant T/A snv 2.0E-02 4
rs128738
P4HA2
0.925 0.160 5 132205182 intron variant G/T snv 0.18 2
rs4252134
PLG
0.925 0.160 6 160732495 intron variant T/C snv 0.21 2
rs762623
CDKN1A ; DINOL
1.000 0.160 6 36677689 non coding transcript exon variant G/A snv 0.12 2
rs10783618
HOXC11 ; HOTAIR
1.000 0.160 12 53971491 intron variant T/C snv 0.51 1
rs2162440 1.000 0.160 18 37634043 intron variant A/G;T snv 1
rs2548861
WWOX
1.000 0.160 16 78624496 intron variant T/G snv 0.52 1
rs6430612 1.000 0.160 2 136248628 intergenic variant C/T snv 0.44 1
rs17435
MECP2
0.851 0.200 X 154046529 intron variant T/A;C snv 4
rs540386
TRAF6
0.851 0.200 11 36503743 intron variant C/G;T snv 4
rs34794968
CD226
0.925 0.200 18 69863790 3 prime UTR variant C/A snv 0.36 2
rs3790567
IL12RB2
0.851 0.240 1 67356694 intron variant A/G snv 0.61 4
rs3218625
PTGS2
0.925 0.240 1 186674409 missense variant C/T snv 1.6E-03 5.0E-04 2
rs2073498
RASSF1
0.763 0.280 3 50332115 missense variant C/A snv 9.6E-02 8.0E-02 12
rs560191
TP53BP1
0.763 0.280 15 43475576 missense variant G/C;T snv 0.36; 4.0E-06 12
rs7025417
LOC107987046 ; IL33
0.752 0.280 9 6240084 intron variant T/C;G snv 11
rs3764340
WWOX
0.807 0.280 16 78432540 missense variant C/G snv 7.1E-02 7.4E-02 9
rs1059702
IRAK1
0.807 0.280 X 154018741 missense variant A/G snv 0.72 7
rs2900180
C5-OT1
0.827 0.280 9 120944104 regulatory region variant T/A;C snv 5
rs3733197
BANK1
0.742 0.320 4 101918130 missense variant G/A snv 0.31 0.30 13
rs1417938
CRP
0.776 0.320 1 159714396 intron variant T/A;C snv 0.28 10
rs3838646
TTTY14
0.827 0.320 Y 18991182 intron variant CA/- del 8
rs6910071
TSBP1 ; TSBP1-AS1
0.790 0.320 6 32315077 intron variant A/G snv 0.14 7
rs7747909
IL17A
0.790 0.320 6 52189451 3 prime UTR variant G/A snv 0.18 7
rs6906021
HLA-DQB1-AS1
0.827 0.320 6 32658534 upstream gene variant T/C snv 0.47 6