Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs113143765
rs113143765
TLR10
1 4 38783103 upstream gene variant -/A delins 0.700 1.000 1 2013 2013
dbSNP: rs11464691
rs11464691 		1 17 40614389 intergenic variant -/A delins 0.68 0.700 1.000 1 2017 2017
dbSNP: rs10663129
rs10663129
RASA2
1 3 141602994 intron variant -/CT delins 0.29 0.700 1.000 1 2017 2017
dbSNP: rs111914382
rs111914382
TTC6
1 14 37627796 intron variant -/G delins 0.20 0.700 1.000 1 2017 2017
dbSNP: rs552531342
rs552531342
IL18R1 ; IL1RL1
1 2 102351127 intron variant -/T delins 0.700 1.000 1 2013 2013
dbSNP: rs150254607
rs150254607 		1 4 122532955 intergenic variant -/TAT ins 4.9E-02 0.700 1.000 1 2017 2017
dbSNP: rs551301661
rs551301661
FAM114A1
1 4 38903573 intron variant -/TT delins 2.1E-05 0.700 1.000 1 2013 2013
dbSNP: rs10455025
rs10455025
TSLP
3 1.000 0.080 5 111069301 upstream gene variant A/C snv 0.24 0.700 1.000 1 2013 2013
dbSNP: rs10497811
rs10497811
PLCL1
1 2 198038185 intron variant A/C snv 0.45 0.700 1.000 1 2013 2013
dbSNP: rs10931791
rs10931791
MARS2
1 2 197708888 intron variant A/C snv 0.29 0.700 1.000 1 2013 2013
dbSNP: rs12440045
rs12440045 		6 0.925 0.080 15 41490486 upstream gene variant A/C snv 0.67 0.700 1.000 1 2017 2017
dbSNP: rs12641669
rs12641669
FAM114A1
1 4 38900148 intron variant A/C snv 0.50 0.700 1.000 1 2013 2013
dbSNP: rs13218331
rs13218331
HLA-DRA
1 6 32443585 intron variant A/C snv 0.13 0.700 1.000 1 2013 2013
dbSNP: rs13270496
rs13270496 		1 8 80368431 intron variant A/C snv 0.49 0.700 1.000 1 2013 2013
dbSNP: rs1342326
rs1342326 		9 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 0.700 1.000 1 2013 2013
dbSNP: rs17599077
rs17599077 		1 6 32623281 upstream gene variant A/C snv 0.10 0.700 1.000 1 2013 2013
dbSNP: rs1870072
rs1870072 		1 5 110846372 intergenic variant A/C snv 0.10 0.700 1.000 1 2013 2013
dbSNP: rs2030517
rs2030517
LPP
1 3 188383915 intron variant A/C snv 0.60 0.700 1.000 1 2013 2013
dbSNP: rs227275
rs227275
MANBA
1 4 102672741 intron variant A/C snv 0.55 0.700 1.000 1 2017 2017
dbSNP: rs2524281
rs2524281 		1 6 31448922 intron variant A/C snv 0.11 0.700 1.000 1 2013 2013
dbSNP: rs2893907
rs2893907
ZNF365
1 10 62622599 intron variant A/C snv 0.65 0.700 1.000 1 2017 2017
dbSNP: rs3763313
rs3763313
BTNL2
7 0.807 0.320 6 32408694 upstream gene variant A/C snv 0.21 0.700 1.000 1 2013 2013
dbSNP: rs4833103
rs4833103
TLR1
5 0.925 0.160 4 38813881 intron variant A/C snv 0.64 0.700 1.000 1 2013 2013
dbSNP: rs56267605
rs56267605 		2 1.000 0.080 4 122441954 intergenic variant A/C snv 0.29 0.700 1.000 1 2018 2018
dbSNP: rs6815814
rs6815814
TLR1
2 1.000 0.080 4 38814717 intron variant A/C snv 0.43 0.700 1.000 1 2013 2013