Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs76886731
IL1RL1 ; IL18R1
1.000 0.040 2 102328956 intron variant A/T snv 0.48 1
rs2058660
IL18RAP
0.882 0.280 2 102437989 intron variant G/A snv 0.78 4
rs77061563
RMI2 ; LOC105371082
1.000 0.040 16 11358685 intron variant C/G;T snv 1
rs10982385 1.000 0.040 9 114730737 intergenic variant T/G snv 0.47 1
rs4574921 0.882 0.160 9 114776054 upstream gene variant C/T snv 0.80 3
rs10114470
TNFSF15
0.882 0.080 9 114785492 3 prime UTR variant T/A;C snv 4
rs6478108
TNFSF15
0.763 0.200 9 114796423 intron variant C/T snv 0.73 10
rs4366152
TNFSF15
1.000 0.040 9 114802595 intron variant T/C snv 0.75 1
rs4979462
TNFSF15
0.790 0.240 9 114804733 intron variant C/T snv 0.13 7
rs6478109
TNFSF15
0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 12
rs10817758
DELEC1
1.000 0.040 9 115381654 intron variant C/T snv 0.13 1
rs10100465
LOC105375721
1.000 0.040 8 117614040 intergenic variant G/A snv 0.23 1
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs55894533 1.000 0.040 8 11891733 downstream gene variant A/C;T snv 1
rs6807915 1.000 0.040 3 12272347 intergenic variant T/C snv 0.65 1
rs3097940
LINC01091
1.000 0.040 4 123863618 non coding transcript exon variant C/T snv 0.48 1
rs8177374
TIRAP
0.672 0.520 11 126292948 missense variant C/T snv 0.12 0.11 22
rs3793964
TOLLIP
0.882 0.120 11 1280752 intron variant T/C snv 0.66 4
rs3811140
FCN2
1.000 0.040 9 134880265 upstream gene variant A/G snv 0.15 1
rs7851696
FCN2
0.827 0.320 9 134887245 missense variant G/C;T snv 0.12 0.14 5
rs13220141 1.000 0.040 6 146576497 intergenic variant A/T snv 8.2E-02 1
rs2275606
LOC101928661 ; ADGB
0.925 0.040 6 146597814 intron variant G/A snv 7.7E-02 2
rs3804099
TLR2
0.627 0.680 4 153703504 synonymous variant T/C snv 0.40 0.48 40
rs121917864
TLR2
0.645 0.520 4 153704936 missense variant C/T snv 8.8E-05 9.8E-05 31
rs295340 1.000 0.040 6 159164909 upstream gene variant A/G snv 0.53 1