Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs151043342 1.000 0.120 6 32453166 intergenic variant C/T snv 1
rs6712572
CKAP2L
1.000 0.120 2 112763101 intron variant G/T snv 0.61 1
rs12722051
HLA-DQA2 ; HLA-DQA1 ; LOC107986589
1.000 0.120 6 32641370 missense variant A/T snv 0.16 0.16 1
rs2071374
IL1A
1.000 0.120 2 112779775 intron variant T/G snv 0.27 1
rs1688075
IL1RN
1.000 0.120 2 113100619 regulatory region variant C/A snv 0.91 1
rs12712122
LINC01127
1.000 0.120 2 101975535 intron variant T/C snv 0.72 1
rs104895179
MEFV
1.000 0.120 16 3254482 missense variant C/A;G;T snv 1.2E-03; 2.5E-05; 4.9E-06 1
rs1279094 0.882 0.120 9 11706771 intron variant T/C snv 0.43 3
rs1823549 0.882 0.120 1 102682275 intergenic variant T/C snv 0.89 3
rs41291794 0.882 0.120 6 32457985 downstream gene variant A/T snv 7.5E-02 3
rs481331 0.882 0.120 10 42507600 intergenic variant A/T snv 0.80 3
rs72632736 0.882 0.120 1 4389144 intergenic variant A/G snv 4.3E-02 3
rs1178121
HDAC9
0.882 0.120 7 18723029 intron variant C/A snv 0.31 3
rs114940806
KLF17
0.882 0.120 1 44093000 intron variant A/G snv 5.4E-02 3
rs12517545
LINC01331
0.882 0.120 5 74384489 intron variant G/A snv 0.13 3
rs864089
PRICKLE2
0.882 0.120 3 64258442 intron variant T/C snv 0.22 3
rs79575701
ZBTB7C
0.882 0.120 18 48053250 intron variant C/A;T snv 3
rs730880295
LACC1
0.851 0.200 13 43883879 missense variant T/C snv 4
rs1479924 0.807 0.120 4 122466445 intergenic variant G/A snv 0.76 6
rs2847293 0.807 0.120 18 12782449 downstream gene variant A/G;T snv 6
rs4648881 0.807 0.120 1 24870664 intergenic variant G/A snv 0.47 6
rs6946509 0.807 0.120 7 22769871 downstream gene variant T/A;C snv 6
rs10213692
ANKRD55
0.807 0.120 5 56146422 intron variant T/C snv 0.17 6
rs79893749
CCR3
0.807 0.120 3 46212159 intron variant C/T snv 0.10 6
rs7069750
FAS
0.807 0.120 10 89002619 non coding transcript exon variant G/C;T snv 0.50 6