Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs7538427
GTF2B
1.000 0.080 1 88873739 intron variant C/T snv 0.93 2
rs1036199
HAVCR2
0.925 0.160 5 157104725 missense variant C/A snv 0.87 0.83 3
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs2816316
LOC105371664
0.882 0.200 1 192567683 intron variant C/A snv 0.79 5
rs638893 0.882 0.080 11 118827828 intergenic variant G/A snv 0.79 4
rs2075184 0.724 0.240 2 102464132 intergenic variant T/C snv 0.78 14
rs951005 0.807 0.200 9 34743684 intron variant G/A snv 0.78 10
rs4761587
PLXNC1
0.882 12 94158023 intron variant A/G snv 0.78 4
rs6498142
CLEC16A
16 10987392 intron variant C/G snv 0.77 3
rs2221903
IL21-AS1 ; IL21
0.752 0.360 4 122617757 intron variant C/T snv 0.77 12
rs548234
ATG5
0.763 0.360 6 106120159 intron variant C/T snv 0.76 11
rs2249937
LOC112267968
1.000 0.080 6 159094277 non coding transcript exon variant T/G snv 0.76 3
rs6478109
TNFSF15
0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 12
rs11711054 1.000 0.080 3 46304120 intergenic variant G/A snv 0.73 2
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs9683415 0.882 4 40290296 regulatory region variant A/G snv 0.71 4
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
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1953126
PHF19
1.000 0.120 9 120878222 intron variant T/C snv 0.68 3
rs7100025
ANKRD30A ; LINC00993
0.724 0.240 10 37303610 intron variant G/A snv 0.68 14
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67 12
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 41