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: rs1800795
rs1800795
IL6 ; STEAP1B ; IL6-AS1
140 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.020 1.000 2 2012 2018
dbSNP: rs4693608
rs4693608
HPSE
6 0.827 0.200 4 83320204 intron variant G/A;C snv 0.020 1.000 2 2010 2014
dbSNP: rs2069727
rs2069727
IFNG ; IFNG-AS1
9 0.763 0.320 12 68154443 intron variant T/A;C snv 0.010 1.000 1 2015 2015
dbSNP: rs2232365
rs2232365
FOXP3
16 0.716 0.480 X 49259429 intron variant T/C snv 0.010 1.000 1 2018 2018
dbSNP: rs2310241
rs2310241
IL1RL2
1 1.000 0.040 2 102225489 intron variant A/C snv 0.44 0.010 1.000 1 2019 2019
dbSNP: rs3092936
rs3092936
CD40LG
2 1.000 0.040 X 136654046 intron variant T/C snv 8.9E-02 0.010 1.000 1 2018 2018
dbSNP: rs337629
rs337629
KLF3-AS1
1 1.000 0.040 4 38633737 intron variant A/G;T snv 0.010 1.000 1 2012 2012
dbSNP: rs352139
rs352139
TLR9
18 0.732 0.320 3 52224356 intron variant T/C snv 0.51 0.54 0.010 1.000 1 2014 2014
dbSNP: rs3761549
rs3761549
FOXP3
18 0.724 0.480 X 49260888 intron variant G/A snv 9.6E-02 0.010 1.000 1 2018 2018
dbSNP: rs41423247
rs41423247
NR3C1
23 0.695 0.440 5 143399010 intron variant G/C snv 0.31 0.010 1.000 1 2015 2015
dbSNP: rs4364254
rs4364254
HPSE
3 0.882 0.080 4 83302560 intron variant C/T snv 0.63 0.010 1.000 1 2010 2010
dbSNP: rs4833079
rs4833079
KLF3-AS1
2 1.000 0.040 4 38653060 intron variant T/C snv 0.30 0.010 1.000 1 2012 2012
dbSNP: rs4845618
rs4845618
IL6R
5 0.851 0.160 1 154427539 intron variant G/T snv 0.53 0.010 1.000 1 2018 2018
dbSNP: rs6531656
rs6531656
KLF3
2 1.000 0.040 4 38682580 intron variant C/T snv 0.87 0.010 1.000 1 2012 2012
dbSNP: rs7588571
rs7588571
REG3A
3 0.882 0.040 2 79161461 intron variant G/A snv 0.49 0.010 < 0.001 1 2017 2017
dbSNP: rs9277378
rs9277378
HLA-DPA1 ; HLA-DPB1
5 0.827 0.320 6 33082502 intron variant A/G snv 0.40 0.010 1.000 1 2017 2017
dbSNP: rs10737416
rs10737416
LOC105373109
1 1.000 0.040 1 224887055 intergenic variant C/A;T snv 0.010 1.000 1 2012 2012
dbSNP: rs4837656
rs4837656 		1 1.000 0.040 9 119671775 intergenic variant T/C snv 0.27 0.010 1.000 1 2012 2012
dbSNP: rs17582214
rs17582214 		1 1.000 0.040 9 119676531 regulatory region variant A/G;T snv 0.010 1.000 1 2012 2012
dbSNP: rs16910526
rs16910526
CLEC7A ; LOC105369655
12 0.742 0.280 12 10118488 stop gained A/C;G snv 6.2E-02 0.010 1.000 1 2010 2010
dbSNP: rs11209026
rs11209026
IL23R
46 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.010 1.000 1 2008 2008
dbSNP: rs1129055
rs1129055
CD86
15 0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25 0.010 1.000 1 2018 2018
dbSNP: rs1217691063
rs1217691063
MTHFR
614 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.010 1.000 1 2009 2009
dbSNP: rs4986791
rs4986791
TLR4
182 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 0.010 1.000 1 2006 2006
dbSNP: rs6195
rs6195
NR3C1
6 0.807 0.120 5 143399752 missense variant T/A;C snv 0.010 1.000 1 2015 2015