Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs77150043
ADCY7
0.724 0.240 16 50270338 intron variant C/T snv 0.17 14
rs2488457
AP4B1-AS1 ; PTPN22
0.763 0.480 1 113872746 intron variant G/A;C snv 11
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 10
rs1004819
C1orf141 ; IL23R
0.776 0.360 1 67204530 intron variant G/A snv 0.30 9
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 9
rs3807306
IRF5
0.776 0.320 7 128940626 intron variant G/A;T snv 8
rs12708716
CLEC16A
0.807 0.320 16 11086016 intron variant A/G snv 0.37 7
rs7234029
PTPN2
0.807 0.320 18 12877061 intron variant A/G snv 0.27 7
rs10931481
STAT4
0.827 0.240 2 191090126 intron variant G/A snv 0.66 5
rs11893432
STAT4
0.827 0.120 2 191057148 intron variant C/G snv 0.21 5
rs2348071
ARMH4 ; PSMA3
0.827 0.240 14 58263908 intron variant A/G snv 0.71 5
rs12917716
CLEC16A
0.851 0.200 16 11095291 intron variant G/C snv 0.51 4
rs17435
MECP2
0.851 0.200 X 154046529 intron variant T/A;C snv 4
rs10761745
JMJD1C
0.882 0.240 10 63341311 intron variant G/C snv 0.87 3
rs10919563
PTPRC
0.925 0.120 1 198731313 intron variant G/A snv 0.21 3
rs2395148
TSBP1 ; TSBP1-AS1
0.882 0.200 6 32353777 intron variant G/T snv 4.6E-02 3
rs2240337
PADI4
0.925 0.200 1 17347727 intron variant C/T snv 9.5E-02 2
rs10128264
ZMIZ1
1.000 0.120 10 79200216 intron variant T/C snv 0.64 1
rs10761744
JMJD1C
1.000 0.120 10 63341266 intron variant C/G;T snv 0.87 1
rs10956445
CCDC26
1.000 0.120 8 128775730 intron variant T/C snv 0.20 1
rs11225055
ANGPTL5
1.000 0.120 11 101900702 intron variant T/A;C snv 1
rs12046117
VTCN1
1.000 0.120 1 117208743 intron variant C/T snv 0.16 1
rs12411988
REEP3
1.000 0.120 10 63555637 intron variant G/C snv 0.12 1
rs12416113
NRBF2
1.000 0.120 10 63136717 intron variant T/A snv 0.13 1
rs12719740
FAM169B
1.000 0.120 15 98529676 intron variant G/A snv 0.21 1