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: rs3824662
rs3824662
11 0.752 0.320 10 8062245 intron variant C/A;T snv 0.700 1.000 3 2013 2018
dbSNP: rs10828317
rs10828317
9 0.776 0.280 10 22550699 missense variant T/C snv 0.700 1.000 2 2013 2018
dbSNP: rs11980379
rs11980379
3 0.882 0.120 7 50402283 3 prime UTR variant T/C snv 0.25 0.700 1.000 2 2013 2017
dbSNP: rs2239633
rs2239633
12 0.742 0.240 14 23119848 upstream gene variant G/A snv 0.38 0.700 1.000 2 2013 2018
dbSNP: rs35837782
rs35837782
2 0.925 0.120 10 124604740 intron variant A/G snv 0.63 0.700 1.000 2 2017 2018
dbSNP: rs3731217
rs3731217
10 0.763 0.320 9 21984662 intron variant A/C;T snv 0.700 1.000 2 2013 2018
dbSNP: rs4762284
rs4762284
1 1.000 0.120 12 96218984 intron variant A/T snv 0.36 0.700 1.000 2 2017 2018
dbSNP: rs189434316
rs189434316
2 0.925 0.120 14 92231568 intergenic variant A/T snv 4.1E-02 0.700 1.000 1 2017 2017
dbSNP: rs28665337
rs28665337
1 1.000 0.120 8 129181858 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs3731249
rs3731249
23 0.683 0.320 9 21970917 missense variant C/A;G;T snv 2.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs4132601
rs4132601
9 0.763 0.240 7 50402906 3 prime UTR variant T/G snv 0.25 0.700 1.000 1 2018 2018
dbSNP: rs7089424
rs7089424
10 0.752 0.200 10 61992400 intron variant T/G snv 0.32 0.700 1.000 1 2018 2018
dbSNP: rs7090445
rs7090445
2 0.925 0.120 10 61961417 intron variant C/G;T snv 0.70 0.700 1.000 1 2013 2013
dbSNP: rs1057519975
rs1057519975
34 0.649 0.480 17 7675209 missense variant A/C;G;T snv 0.010 1.000 1 2003 2003
dbSNP: rs1287276985
rs1287276985
7 0.790 0.200 6 43782020 missense variant T/A;C snv 4.0E-06; 4.0E-06 7.0E-06 0.010 1.000 1 2003 2003
dbSNP: rs156697
rs156697
25 0.672 0.560 10 104279427 missense variant A/G;T snv 0.35 0.010 < 0.001 1 2015 2015
dbSNP: rs2393732
rs2393732
2 0.925 0.120 10 62007470 intron variant G/A snv 0.15 0.010 < 0.001 1 2019 2019
dbSNP: rs4925
rs4925
28 0.677 0.560 10 104263031 missense variant C/A snv 0.25 0.23 0.010 < 0.001 1 2015 2015
dbSNP: rs4948488
rs4948488
2 0.925 0.120 10 61925395 intron variant C/A;T snv 0.010 < 0.001 1 2019 2019
dbSNP: rs62527607
rs62527607
5 0.827 0.160 8 103141321 non coding transcript exon variant G/T snv 0.14 0.010 1.000 1 2017 2017
dbSNP: rs866838052
rs866838052
6 0.851 0.160 7 143267618 missense variant C/A snv 0.010 < 0.001 1 2015 2015