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: rs10994982
rs10994982
ARID5B
7 0.790 0.120 10 61950345 intron variant A/G snv 0.49 0.030 0.667 3 2014 2019
dbSNP: rs3731217
rs3731217
CDKN2A
10 0.763 0.320 9 21984662 intron variant A/C;T snv 0.030 1.000 3 2010 2018
dbSNP: rs4938723
rs4938723
BTG4 ; MIR34B ; MIR34C ; LOC728196
60 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.030 1.000 3 2016 2019
dbSNP: rs10821936
rs10821936
ARID5B
11 0.742 0.200 10 61963818 intron variant C/T snv 0.69 0.020 1.000 2 2014 2019
dbSNP: rs11978267
rs11978267
IKZF1
9 0.763 0.240 7 50398606 intron variant A/G snv 0.25 0.020 1.000 2 2017 2019
dbSNP: rs3824662
rs3824662
GATA3
11 0.752 0.320 10 8062245 intron variant C/A;T snv 0.020 1.000 2 2013 2017
dbSNP: rs7088318
rs7088318
PIP4K2A
4 0.851 0.120 10 22564019 intron variant C/A snv 0.55 0.020 1.000 2 2013 2016
dbSNP: rs924607
rs924607
LOC100996325 ; LOC105374608
7 0.851 0.120 5 609978 intron variant C/T snv 0.32 0.020 1.000 2 2016 2019
dbSNP: rs10235796
rs10235796
IKZF1
3 0.882 0.120 7 50394939 intron variant T/C snv 0.82 0.010 1.000 1 2017 2017
dbSNP: rs10519612
rs10519612
IL15
3 0.882 0.120 4 141732548 intron variant A/C snv 0.10 0.010 1.000 1 2015 2015
dbSNP: rs10740055
rs10740055
ARID5B
7 0.790 0.240 10 61958720 intron variant C/A snv 0.49 0.010 1.000 1 2017 2017
dbSNP: rs10853104
rs10853104
IGF2BP1
1 1.000 0.120 17 49014714 intron variant C/G;T snv 0.010 1.000 1 2019 2019
dbSNP: rs111978267
rs111978267
KCNQ1
3 0.882 0.120 11 2751648 intron variant C/G;T snv 2.8E-05 0.010 1.000 1 2019 2019
dbSNP: rs153109
rs153109
IL27
37 0.623 0.600 16 28507775 intron variant T/C snv 0.43 0.010 1.000 1 2018 2018
dbSNP: rs1544105
rs1544105
FPGS
4 0.851 0.200 9 127800446 intron variant C/T snv 0.48 0.010 1.000 1 2015 2015
dbSNP: rs17069665
rs17069665
FOXO3
4 0.882 0.120 6 108620265 intron variant A/C;G snv 0.010 1.000 1 2020 2020
dbSNP: rs17213693
rs17213693
HLA-DOB
2 0.925 0.120 6 32813344 intron variant G/C snv 9.8E-02 0.010 1.000 1 2019 2019
dbSNP: rs1966862
rs1966862
ARHGAP24
8 0.790 0.120 4 85766908 intron variant A/G snv 0.14 0.010 1.000 1 2010 2010
dbSNP: rs2036914
rs2036914
F11
5 0.882 0.160 4 186271327 intron variant T/C snv 0.57 0.010 1.000 1 2019 2019
dbSNP: rs2069727
rs2069727
IFNG ; IFNG-AS1
9 0.763 0.320 12 68154443 intron variant T/A;C snv 0.010 1.000 1 2010 2010
dbSNP: rs210143
rs210143
BAK1 ; GGNBP1
6 0.827 0.160 6 33579153 intron variant T/C snv 0.74 0.010 1.000 1 2019 2019
dbSNP: rs2413739
rs2413739
PACSIN2
6 0.827 0.120 22 43001030 intron variant C/T snv 0.43 0.010 1.000 1 2019 2019
dbSNP: rs2430561
rs2430561
IFNG ; IFNG-AS1
50 0.590 0.760 12 68158742 intron variant T/A snv 0.36 0.010 1.000 1 2018 2018
dbSNP: rs3731246
rs3731246
CDKN2A
3 0.882 0.120 9 21971990 intron variant C/G snv 0.11 0.010 1.000 1 2017 2017
dbSNP: rs3794012
rs3794012
LMO1
3 0.882 0.120 11 8248697 intron variant T/C snv 0.32 0.010 1.000 1 2017 2017