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: rs3184504
rs3184504
92 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 0.720 1.000 2 2014 2017
dbSNP: rs6000782
rs6000782
2 0.925 0.080 22 37532179 intergenic variant A/C snv 0.15 0.020 1.000 2 2014 2019
dbSNP: rs11065904
rs11065904
4 0.882 0.080 12 111449163 3 prime UTR variant T/A snv 3.2E-02 0.010 1.000 1 2017 2017
dbSNP: rs121434254
rs121434254
6 0.807 0.200 21 44289773 stop gained C/A;T snv 7.5E-04 0.010 1.000 1 2001 2001
dbSNP: rs1799724
rs1799724
LTA ; TNF
47 0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 0.010 1.000 1 2019 2019
dbSNP: rs1800871
rs1800871
108 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 0.010 1.000 1 2018 2018
dbSNP: rs1800872
rs1800872
119 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 0.010 1.000 1 2018 2018
dbSNP: rs2069762
rs2069762
IL2
23 0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 0.010 < 0.001 1 2018 2018
dbSNP: rs2069763
rs2069763
IL2
6 0.807 0.320 4 122456327 synonymous variant C/A snv 0.36 0.29 0.010 1.000 1 2018 2018
dbSNP: rs2187668
rs2187668
20 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 0.710 1.000 1 2014 2014
dbSNP: rs2238154
rs2238154
4 0.882 0.080 12 111444681 intron variant C/A;G snv 0.010 1.000 1 2017 2017
dbSNP: rs231775
rs231775
115 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.010 1.000 1 2015 2015
dbSNP: rs2476601
rs2476601
121 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.010 1.000 1 2017 2017
dbSNP: rs2488458
rs2488458
2 0.925 0.080 1 113863829 intron variant T/A;C snv 0.010 1.000 1 2016 2016
dbSNP: rs3891175
rs3891175
5 0.851 0.160 6 32666690 5 prime UTR variant C/T snv 0.20 0.700 1.000 1 2018 2018
dbSNP: rs4325730
rs4325730
2 0.925 0.080 2 203933067 upstream gene variant G/A;T snv 0.010 1.000 1 2017 2017
dbSNP: rs739496
rs739496
10 0.790 0.160 12 111449855 3 prime UTR variant A/G snv 0.27 0.010 1.000 1 2017 2017
dbSNP: rs755622
rs755622
44 0.611 0.720 22 23894205 intron variant G/C snv 0.26 0.010 < 0.001 1 2016 2016
dbSNP: rs7574865
rs7574865
59 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.010 1.000 1 2017 2017
dbSNP: rs7582694
rs7582694
9 0.763 0.400 2 191105394 intron variant C/G snv 0.77 0.010 1.000 1 2017 2017
dbSNP: rs7708392
rs7708392
13 0.732 0.400 5 151077924 intron variant G/C snv 0.44 0.010 1.000 1 2018 2018
dbSNP: rs9277534
rs9277534
7 0.790 0.280 6 33087030 3 prime UTR variant A/G snv 0.38 0.010 1.000 1 2018 2018
dbSNP: rs5844572
rs5844572
11 0.752 0.360 22 23893562 intron variant -/ATTC delins 0.010 1.000 1 2014 2014