Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10202630 0.882 2 190398199 intergenic variant T/C snv 0.52 4
rs1020388 5 56264200 upstream gene variant T/G snv 0.34 2
rs10272724 0.882 0.200 7 50409515 downstream gene variant T/C snv 0.24 4
rs1032129
TNFRSF11B
0.851 0.040 8 118939661 intron variant A/C snv 0.37 5
rs1036199
HAVCR2
0.925 0.160 5 157104725 missense variant C/A snv 0.87 0.83 3
rs10425559 0.807 0.040 19 4837475 upstream gene variant A/G snv 0.66 7
rs10444776
LOC112268138
0.882 14 105647030 upstream gene variant G/A;T snv 4
rs10460003
LINC01882
18 12747013 intron variant C/T snv 0.15 2
rs10488631
TNPO3
0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 13
rs104895271
TNFRSF1A
0.851 0.240 12 6334161 missense variant A/C;G snv 1.6E-04; 4.8E-05 6
rs1049353
CNR1
0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs10494079
VAV3
0.882 1 107832253 intron variant G/C snv 9.0E-02 4
rs1050501
FCGR2B
0.732 0.440 1 161674008 missense variant T/C snv 0.16 0.19 15
rs10516487
BANK1
0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 11
rs1052237
NUS1
6 117694118 stop gained T/C;G snv 8.8E-05 8.4E-05 1
rs1053874
DNASE1 ; TRAP1
0.851 0.240 16 3657746 missense variant G/A;T snv 0.36; 4.0E-06 7
rs1059702
IRAK1
0.807 0.280 X 154018741 missense variant A/G snv 0.72 7
rs1059703
IRAK1
0.851 0.280 X 154013378 missense variant G/A snv 0.67 6
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33
rs10735810
VDR
0.662 0.640 12 47879112 start lost A/C;G;T snv 26
rs10748781 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 11
rs10752747
MMEL1
1 2593476 intron variant G/T snv 0.41 2
rs10797431
LOC100996583
0.851 0.080 1 2569783 non coding transcript exon variant G/T snv 0.42 5
rs10806425
BACH2
0.851 0.280 6 90216893 intron variant C/A snv 0.33 6
rs10822050 0.724 0.240 10 62679011 downstream gene variant T/C snv 0.33 14