Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4149570
TNFRSF1A
0.752 0.360 12 6342424 upstream gene variant A/C;G;T snv 11
rs878859113
CD24
0.763 0.360 6 106971734 missense variant G/A snv 0.35 11
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 10
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 10
rs477515
HLA-DRB1
0.790 0.400 6 32601914 intergenic variant G/A snv 0.27 10
rs4845604
RORC
0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
rs6478108
TNFSF15
0.763 0.200 9 114796423 intron variant C/T snv 0.73 10
rs7495132
CRTC3 ; CRTC3-AS1
0.790 0.080 15 90629669 intron variant C/T snv 0.12 10
rs1004819
C1orf141 ; IL23R
0.776 0.360 1 67204530 intron variant G/A snv 0.30 9
rs11168249
HDAC7
0.807 0.120 12 47814585 intron variant T/C snv 0.50 9
rs12343867
INSL6 ; JAK2
0.790 0.200 9 5074189 intron variant T/C snv 0.25 9
rs2266959
UBE2L3
0.776 0.200 22 21568615 intron variant G/T snv 0.18 9
rs2284553
IFNGR2
0.776 0.240 21 33404389 intron variant A/G snv 0.69 9
rs26528
IL27
0.807 0.200 16 28506388 intron variant T/C snv 0.43 9
rs3024493
IL19 ; IL10
0.776 0.280 1 206770623 intron variant C/A;T snv 0.11 9
rs34920465 0.807 0.160 1 22373858 intergenic variant A/G snv 0.24 9
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 9
rs11236797 0.790 0.200 11 76588605 upstream gene variant C/A snv 0.39 8
rs1182188
GNA12
0.827 0.120 7 2830351 intron variant T/C snv 0.26 8
rs1457092
MYO9B
0.790 0.320 19 17193427 intron variant C/A snv 0.44 8
rs1495965 0.790 0.280 1 67287825 intergenic variant C/T snv 0.55 8
rs17622378
IRF1-AS1
0.790 0.200 5 132442760 intron variant A/G snv 0.28 8
rs212388
LOC112267968 ; LOC105378083
0.827 0.240 6 159069404 intron variant C/G;T snv 8
rs4958847
IRGM
0.807 0.120 5 150860025 intron variant G/A snv 0.25 8
rs6651252
LINC00824
0.790 0.200 8 128554935 intron variant T/C snv 0.19 8