Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1275561861
HLA-A
0.672 0.360 6 29944350 missense variant G/A snv 23
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 16
rs62324212
IL21-AS1
0.724 0.240 4 122639784 intron variant C/A;G snv 15
rs10988542
FNBP1
0.724 0.240 9 129894985 intron variant G/A;C snv 14
rs11145763
CARD9
0.724 0.240 9 136369144 intron variant A/C;G;T snv 14
rs11580078
C1orf141 ; IL23R
0.724 0.240 1 67203951 intron variant C/A;G snv 14
rs1332099 0.724 0.240 10 99538694 downstream gene variant T/C;G snv 14
rs2738774 0.724 0.240 20 63637985 downstream gene variant G/A;C snv 14
rs2807264 0.724 0.240 X 136583619 downstream gene variant C/A snv 14
rs4869313
ERAP2 ; ERAP1
0.724 0.240 5 96888176 intron variant T/A;G snv 14
rs55705316 0.724 0.240 1 206760172 regulatory region variant T/A;G snv 14
rs7660520 0.724 0.240 4 182824168 upstream gene variant G/A;C snv 14
rs7831697 0.724 0.240 8 137124061 regulatory region variant T/A;C;G snv 14
rs72553883
TNFRSF13B
0.851 0.080 17 16940415 missense variant G/A;T snv 2.8E-05; 5.3E-03 5
rs10127016
KANTR
1.000 0.040 X 53122914 intron variant G/T snv 1
rs1926283
GNG12-AS1
1.000 0.040 1 67982978 intron variant A/G;T snv 1
rs2682665 1.000 0.040 8 13940496 intergenic variant C/A;T snv 1
rs375099
RANBP2
1.000 0.040 2 109043821 intergenic variant G/A;C snv 1
rs4765961
CACNA1C
1.000 0.040 12 2559306 intron variant T/C;G snv 1
rs5918500
SRPX
1.000 0.040 X 38209996 intron variant C/T snv 1
rs5987017
ATP2B3
1.000 0.040 X 153516714 upstream gene variant A/G snv 1
rs746054383
ICOS
1.000 0.040 2 203956670 missense variant T/C snv 4.0E-06 1
rs748910652
NFKB2
1.000 0.040 10 102400759 stop gained C/T snv 8.2E-06 1
rs774837924
CD40
1.000 0.040 20 46128901 missense variant A/C snv 4.0E-06 1
rs751216929
TNFRSF13B
1.000 0.040 17 16940442 missense variant C/T snv 1.8E-04 2.0E-04 1