Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113143765
TLR10
4 38783103 upstream gene variant -/A delins 1
rs11464691 17 40614389 intergenic variant -/A delins 0.68 1
rs10663129
RASA2
3 141602994 intron variant -/CT delins 0.29 1
rs111914382
TTC6
14 37627796 intron variant -/G delins 0.20 1
rs552531342
IL18R1 ; IL1RL1
2 102351127 intron variant -/T delins 1
rs150254607 4 122532955 intergenic variant -/TAT ins 4.9E-02 1
rs551301661
FAM114A1
4 38903573 intron variant -/TT delins 2.1E-05 1
rs1342326 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 9
rs848
IL13 ; TH2LCRR
0.807 0.240 5 132660808 3 prime UTR variant A/C snv 0.67 8
rs3763313
BTNL2
0.807 0.320 6 32408694 upstream gene variant A/C snv 0.21 7
rs12440045 0.925 0.080 15 41490486 upstream gene variant A/C snv 0.67 6
rs4833103
TLR1
0.925 0.160 4 38813881 intron variant A/C snv 0.64 5
rs7751505 1.000 6 31392478 downstream gene variant A/C snv 0.31 5
rs10455025
TSLP
1.000 0.080 5 111069301 upstream gene variant A/C snv 0.24 3
rs56267605 1.000 0.080 4 122441954 intergenic variant A/C snv 0.29 2
rs6815814
TLR1
1.000 0.080 4 38814717 intron variant A/C snv 0.43 2
rs10497811
PLCL1
2 198038185 intron variant A/C snv 0.45 1
rs10931791
MARS2
2 197708888 intron variant A/C snv 0.29 1
rs12641669
FAM114A1
4 38900148 intron variant A/C snv 0.50 1
rs13218331
HLA-DRA
6 32443585 intron variant A/C snv 0.13 1
rs13270496 8 80368431 intron variant A/C snv 0.49 1
rs17599077 6 32623281 upstream gene variant A/C snv 0.10 1
rs1870072 5 110846372 intergenic variant A/C snv 0.10 1
rs2030517
LPP
3 188383915 intron variant A/C snv 0.60 1
rs227275
MANBA
4 102672741 intron variant A/C snv 0.55 1