Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs559928 0.827 0.120 11 64382898 intergenic variant T/C snv 0.77 6
rs7313895
LRRK2
0.827 0.120 12 40350592 intron variant G/T snv 0.77 5
rs4833837
IL21
0.827 0.200 4 122615808 synonymous variant G/A snv 0.74 0.77 5
rs6548123
MYT1L
0.925 0.120 2 2221629 intron variant C/T snv 0.76 2
rs10088247
CSMD1
1.000 0.040 8 3826677 intron variant C/T snv 0.76 1
rs482160
PTPN2
1.000 0.040 18 12855647 intron variant A/G snv 0.76 1
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs2451258
LOC112267968
0.807 0.160 6 159085568 intron variant C/T snv 0.75 6
rs7007032
CSMD1
1.000 0.040 8 3821924 intron variant C/T snv 0.75 1
rs6478109
TNFSF15
0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 12
rs7848647
TNFSF15
0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74 13
rs3751385
GJB2
1.000 0.040 13 20188817 3 prime UTR variant A/G snv 0.74 1
rs12075255
IL19
0.827 0.120 1 206788283 intron variant A/G snv 0.74 5
rs6478108
TNFSF15
0.763 0.200 9 114796423 intron variant C/T snv 0.73 10
rs9807841
QTRT1
1.000 0.040 19 10706980 intron variant T/C snv 0.73 1
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2066363
ADGRL2
0.724 0.240 1 81771892 intron variant C/T snv 0.71 14
rs2944542
ZNF365
0.925 0.120 10 62610240 intron variant C/G snv 0.71 2
rs2357623 0.827 0.120 16 50660100 upstream gene variant A/G snv 0.71 5
rs2787094
ADAM33
0.851 0.160 20 3668514 3 prime UTR variant C/G snv 0.71 4
rs27044
ERAP1 ; LOC102724748
0.827 0.240 5 96783148 missense variant G/C snv 0.69 0.71 5
rs9513593
GPR183 ; UBAC2
1.000 0.040 13 99298006 intron variant G/A snv 0.71 1
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs643177
TNFAIP3
1.000 0.040 6 137874556 intron variant T/C snv 0.70 1