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: rs2241339
rs2241339
3 2 169013785 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs2371605
rs2371605
1 3 29256913 intron variant G/A snv 4.6E-02 0.700 1.000 1 2019 2019
dbSNP: rs2489201
rs2489201
1 10 18221519 intron variant G/A snv 0.62 0.700 1.000 1 2018 2018
dbSNP: rs2491441
rs2491441
1 1 183833125 intron variant T/C snv 0.16 0.700 1.000 1 2018 2018
dbSNP: rs2896019
rs2896019
10 0.790 0.160 22 43937814 intron variant T/G snv 0.20 0.700 1.000 1 2010 2010
dbSNP: rs319991
rs319991
1 1 48651222 intron variant G/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs333947
rs333947
7 1 109928142 intron variant G/A snv 0.13 0.700 1.000 1 2018 2018
dbSNP: rs34010237
rs34010237
3 19 49509317 intron variant G/A snv 0.13 0.700 1.000 1 2018 2018
dbSNP: rs34173
rs34173
1 7 31695649 intron variant G/C snv 0.70 0.75 0.700 1.000 1 2019 2019
dbSNP: rs3747207
rs3747207
7 22 43928975 intron variant G/A snv 0.22 0.700 1.000 1 2019 2019
dbSNP: rs4598207
rs4598207
2 7 50218883 intron variant A/T snv 0.34 0.700 1.000 1 2018 2018
dbSNP: rs4823173
rs4823173
8 0.827 0.200 22 43932850 intron variant G/A snv 0.24 0.18 0.700 1.000 1 2019 2019
dbSNP: rs4835265
rs4835265
6 4 145900258 intron variant C/A snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs4949718
rs4949718
3 1 76433779 intron variant T/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs596406
rs596406
1 10 11182702 intron variant T/C snv 0.15 0.700 1.000 1 2013 2013
dbSNP: rs6455128
rs6455128
2 1.000 0.080 6 61987841 intron variant A/C snv 0.79 0.700 1.000 1 2008 2008
dbSNP: rs686288
rs686288
1 12 100982873 intron variant A/G snv 4.6E-02 0.700 1.000 1 2019 2019
dbSNP: rs6899983
rs6899983
1 6 31791154 intron variant A/C snv 3.3E-02 0.700 1.000 1 2019 2019
dbSNP: rs7043196
rs7043196
1 9 114371911 intron variant C/T snv 0.43 0.700 1.000 1 2018 2018
dbSNP: rs72838936
rs72838936
1 10 98480617 intron variant C/T snv 9.4E-02 0.700 1.000 1 2018 2018
dbSNP: rs73154660
rs73154660
1 3 157229738 intron variant A/G snv 1.7E-02 0.700 1.000 1 2019 2019
dbSNP: rs73550818
rs73550818
1 16 58730951 intron variant C/A snv 0.12 0.700 1.000 1 2018 2018
dbSNP: rs74913549
rs74913549
3 11 94180526 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs76053346
rs76053346
1 10 110996333 intron variant G/T snv 2.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs76622665
rs76622665
1 5 65395057 intron variant T/C snv 9.3E-03 0.700 1.000 1 2019 2019