Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12212067
FOXO3
0.716 0.320 6 108659993 intron variant T/G snv 0.14 20
rs1463502008
PRH1-PRR4 ; PRH1 ; PRH2 ; PRR4
0.925 0.040 12 10930275 missense variant G/C snv 4.0E-06 2
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs8177374
TIRAP
0.672 0.520 11 126292948 missense variant C/T snv 0.12 0.11 22
rs1881457
IL13 ; TH2LCRR
0.790 0.280 5 132656717 intron variant A/C snv 0.21 9
rs1800925
IL13 ; TH2LCRR
0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs2070874
IL4
0.672 0.560 5 132674018 5 prime UTR variant C/T snv 0.28 0.28 27
rs2243267
IL4
0.882 0.160 5 132678194 intron variant G/A;C snv 3
rs2243268
IL4
0.882 0.040 5 132678271 intron variant A/C snv 0.23 3
rs8179190
LOC105379176 ; IL4
1.000 0.040 5 132680584 intron variant AAGCAAGATGGCCTGTTGGGAGGCTACCACAGTAAACCAGGCTAGAGACGATGGTGGCGTGGACAGAATGAAGCAAGATGGCCTGTTGGGAGGCTACCACAGTAAACCAGGCTAGAGATGATGGTGGCGTGGACAGAATG/- delins 1
rs2243282
IL4 ; LOC105379176
1.000 0.040 5 132680862 intron variant C/A;T snv 1
rs5744454
TMCO6 ; CD14
1.000 0.040 5 140633982 upstream gene variant T/C;G snv 1
rs76723693
G6PD
0.882 0.160 X 154533025 missense variant A/G snv 5.3E-04 1.5E-03 3
rs17860508
LOC285626
0.752 0.360 5 159333192 intron variant TTAGAG/GC delins 11
rs762513613
FCGR2C
0.752 0.280 1 161591315 missense variant A/G snv 4.2E-06 7.4E-06 11
rs34383331
MIF-AS1
0.882 0.040 22 23895892 non coding transcript exon variant T/A snv 0.19 0.18 3
rs9624472
ADORA2A ; ADORA2A-AS1 ; SPECC1L-ADORA2A
0.925 0.040 22 24438763 splice region variant A/G snv 0.10 2
rs9282801
NOS2
1.000 0.040 17 27769447 intron variant C/A snv 0.32 1
rs1799964
LTA ; LOC100287329 ; TNF
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs1800630
TNF ; LOC100287329 ; LTA
0.701 0.480 6 31574699 upstream gene variant C/A snv 0.14 17
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs1046089
PRRC2A
0.882 0.200 6 31635190 missense variant G/A snv 0.36 0.40 4
rs2257167
IFNAR1
0.807 0.200 21 33343393 missense variant G/C snv 0.18 0.16 7
rs867186
PROCR ; MMP24-AS1-EDEM2
0.752 0.120 20 35176751 missense variant A/G snv 0.10 9.7E-02 15