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: rs398652
rs398652
10 0.752 0.240 14 56058851 intergenic variant G/A snv 0.24 0.020 1.000 2 2013 2014
dbSNP: rs10484761
rs10484761
7 0.807 0.080 6 40834522 intergenic variant T/C snv 0.31 0.010 1.000 1 2014 2014
dbSNP: rs10811474
rs10811474
11 0.742 0.240 9 21114238 intergenic variant A/G snv 0.44 0.010 1.000 1 2014 2014
dbSNP: rs10811661
rs10811661
22 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 0.010 1.000 1 2019 2019
dbSNP: rs12894364
rs12894364
1 1.000 0.080 14 37588860 downstream gene variant C/T snv 7.6E-02 0.010 1.000 1 2016 2016
dbSNP: rs1679013
rs1679013
3 0.882 0.160 9 22206988 intron variant C/A;T snv 0.43 0.010 1.000 1 2017 2017
dbSNP: rs1924966
rs1924966
6 0.807 0.080 13 72432915 intergenic variant T/G snv 0.33 0.010 1.000 1 2015 2015
dbSNP: rs2270628
rs2270628
2 0.925 0.120 7 45909971 downstream gene variant C/T snv 0.25 0.010 1.000 1 2014 2014
dbSNP: rs2294750
rs2294750
1 1.000 0.080 1 10824979 regulatory region variant G/A snv 0.10 0.010 1.000 1 2016 2016
dbSNP: rs2477137
rs2477137
1 1.000 0.080 1 17304110 upstream gene variant G/T snv 0.20 0.010 1.000 1 2017 2017
dbSNP: rs2736108
rs2736108
6 0.807 0.160 5 1297373 upstream gene variant C/T snv 0.24 0.010 1.000 1 2017 2017
dbSNP: rs2764736
rs2764736
4 0.851 0.160 9 25067733 intergenic variant T/C snv 2.4E-02 0.010 1.000 1 2014 2014
dbSNP: rs2844695
rs2844695
1 1.000 0.080 6 30968237 intergenic variant T/C snv 0.28 0.010 1.000 1 2014 2014
dbSNP: rs2904268
rs2904268
1 1.000 0.080 20 50433551 upstream gene variant C/A;G snv 0.010 1.000 1 2017 2017
dbSNP: rs35399661
rs35399661
1 1.000 0.080 6 32623213 upstream gene variant T/C snv 0.16 0.010 1.000 1 2014 2014
dbSNP: rs35597309
rs35597309
2 0.925 0.120 6 32621489 regulatory region variant G/A snv 4.8E-02 0.700 1.000 1 2014 2014
dbSNP: rs3763338
rs3763338
1 1.000 0.080 6 28926534 upstream gene variant G/A snv 0.11 0.010 1.000 1 2014 2014
dbSNP: rs6854472
rs6854472
1 1.000 0.080 4 89513521 intron variant G/T snv 0.30 0.010 < 0.001 1 2019 2019
dbSNP: rs7578456
rs7578456
2 1.000 0.080 2 201370625 intergenic variant A/G snv 0.57 0.010 1.000 1 2019 2019
dbSNP: rs2032582
rs2032582
97 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1.000 1 2019 2019
dbSNP: rs1800682
rs1800682
32 0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 0.010 1.000 1 2011 2011
dbSNP: rs2234767
rs2234767
30 0.649 0.280 10 88989499 intron variant G/A;T snv 0.15 0.010 1.000 1 2011 2011
dbSNP: rs1229984
rs1229984
83 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 0.080 1.000 8 2009 2019
dbSNP: rs1042026
rs1042026
2 1.000 0.080 4 99307309 3 prime UTR variant T/C snv 0.24 0.010 1.000 1 2019 2019
dbSNP: rs1614972
rs1614972
4 0.925 0.160 4 99336998 intron variant C/T snv 0.38 0.010 1.000 1 2014 2014