Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113010607
SEPTIN8
0.925 0.080 5 132770006 intron variant T/C snv 0.21 2
rs12081541 0.925 0.160 1 152468890 intergenic variant T/C snv 8.9E-02 2
rs1696361 0.925 0.080 12 120926020 TF binding site variant T/C snv 0.75 2
rs2450083
COLEC10
1.000 0.080 8 119051303 intron variant T/C snv 0.59 2
rs274943
LOC101929563
0.925 0.080 9 23585841 intron variant T/C snv 0.48 2
rs4795399
GSDMB
0.925 0.080 17 39905186 intron variant T/C snv 0.35 2
rs4988958
IL1RL1 ; IL18R1
1.000 0.080 2 102351825 synonymous variant T/C snv 0.34 0.46 2
rs67551275
SPSB1
0.925 0.080 1 9296617 intron variant T/C snv 0.43 2
rs766736182
IL7
0.925 0.080 8 78733724 missense variant T/C snv 4.2E-06 2
rs8066582
PSMD3
0.925 0.080 17 39990676 intron variant T/C snv 0.56 2
rs8079416
LRRC3C
0.925 0.080 17 39936460 intron variant T/C snv 0.45 2
rs943451
PRKCQ-AS1 ; PRKCQ
0.925 0.080 10 6579811 intron variant T/C snv 0.51 2
rs9916279
PSMD3
0.925 0.080 17 39989901 synonymous variant T/C snv 0.14 0.21 2
rs10519031 1.000 0.080 15 59890806 regulatory region variant T/C snv 2.2E-02 1
rs17218161 1.000 0.080 4 58347679 intergenic variant T/C snv 4.3E-03 1
rs3893044 1.000 0.080 17 39946763 downstream gene variant T/C snv 0.63 1
rs4473914
ITGB8
1.000 0.080 7 20386640 intron variant T/C snv 0.37 1
rs6054973 1.000 0.080 20 7405311 intergenic variant T/C snv 4.8E-02 1
rs7045156 1.000 0.080 9 79311350 intergenic variant T/C snv 3.6E-02 1
rs917115
JAZF1
1.000 0.080 7 28132967 intron variant T/C snv 0.41 1
rs10924993 0.925 0.080 1 236296485 intergenic variant T/A;G snv 2
rs4795405
LRRC3C
0.851 0.160 17 39932164 intron variant T/A;C snv 6
rs2428494
HLA-B
0.827 0.160 6 31354420 intron variant T/A;C snv 5
rs72823641
IL1RL1 ; IL18R1
0.882 0.080 2 102319699 intron variant T/A;C snv 4
rs8065126
LRRC3C
1.000 0.080 17 39942782 intron variant T/A;C snv 2