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: rs8066582
rs8066582
2 0.925 0.080 17 39990676 intron variant T/C snv 0.56 0.010 < 0.001 1 2016 2016
dbSNP: rs9916279
rs9916279
2 0.925 0.080 17 39989901 synonymous variant T/C snv 0.14 0.21 0.010 < 0.001 1 2016 2016
dbSNP: rs528557
rs528557
6 0.827 0.120 20 3671095 synonymous variant C/A;G snv 4.7E-06; 0.29 0.020 0.500 2 2015 2017
dbSNP: rs2305480
rs2305480
10 0.763 0.280 17 39905943 missense variant G/A snv 0.40 0.35 0.820 0.750 4 2007 2016
dbSNP: rs7216389
rs7216389
14 0.732 0.440 17 39913696 intron variant C/T snv 0.60 0.080 1.000 8 2008 2018
dbSNP: rs6967330
rs6967330
8 0.827 0.120 7 106018005 missense variant G/A snv 0.19 0.21 0.740 1.000 5 2014 2019
dbSNP: rs479844
rs479844
6 0.851 0.160 11 65784486 upstream gene variant A/G snv 0.44 0.700 1.000 3 2015 2019
dbSNP: rs1042713
rs1042713
63 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 0.020 1.000 2 2013 2016
dbSNP: rs11071559
rs11071559
4 0.925 0.080 15 60777789 intron variant C/T snv 0.23 0.700 1.000 2 2019 2019
dbSNP: rs12023876
rs12023876
2 0.925 0.080 1 203124073 intron variant G/A;T snv 0.700 1.000 2 2019 2019
dbSNP: rs12365699
rs12365699
5 0.882 0.120 11 118872577 regulatory region variant G/A snv 0.12 0.700 1.000 2 2019 2019
dbSNP: rs12964116
rs12964116
2 0.925 0.080 18 63775385 5 prime UTR variant A/G snv 3.0E-02 0.700 1.000 2 2019 2019
dbSNP: rs13277355
rs13277355
3 0.882 0.120 8 127765473 intergenic variant A/G snv 0.71 0.700 1.000 2 2019 2019
dbSNP: rs16903574
rs16903574
6 0.882 0.120 5 14610200 missense variant C/A;G snv 4.0E-06; 5.6E-02 0.700 1.000 2 2019 2019
dbSNP: rs1695
rs1695
188 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.020 1.000 2 2007 2010
dbSNP: rs1837253
rs1837253
10 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 0.700 1.000 2 2019 2019
dbSNP: rs1887704
rs1887704
2 0.925 0.080 13 99322238 intron variant C/G snv 0.55 0.700 1.000 2 2019 2019
dbSNP: rs2066844
rs2066844
54 0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02 0.700 1.000 2 2019 2019
dbSNP: rs2243250
rs2243250
IL4
61 0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 0.020 1.000 2 2015 2016
dbSNP: rs2275913
rs2275913
105 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.020 1.000 2 2010 2018
dbSNP: rs3122929
rs3122929
4 0.882 0.080 12 57115319 intron variant C/T snv 0.33 0.700 1.000 2 2019 2019
dbSNP: rs34290285
rs34290285
8 0.851 0.120 2 241759225 intron variant G/A snv 0.27 0.700 1.000 2 2019 2019
dbSNP: rs35570272
rs35570272
2 0.925 0.080 3 33006170 intron variant G/T snv 0.36 0.700 1.000 2 2019 2019
dbSNP: rs3785356
rs3785356
5 0.925 0.080 16 27337847 intron variant C/T snv 0.25 0.700 1.000 2 2019 2019
dbSNP: rs3894194
rs3894194
3 0.882 0.120 17 39965740 missense variant G/A snv 0.46 0.41 0.800 1.000 2 2007 2014