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: rs1420101
rs1420101
8 0.827 0.280 2 102341256 synonymous variant C/T snv 0.33 0.35 0.800 1.000 1 2009 2009
dbSNP: rs2416257
rs2416257
5 0.882 0.160 5 111099792 intron variant C/G;T snv 0.800 1.000 1 2009 2009
dbSNP: rs2516399
rs2516399
3 0.925 0.120 6 31513522 upstream gene variant A/G snv 0.11 0.800 1.000 1 2011 2011
dbSNP: rs331615
rs331615
1 20 57063481 intergenic variant T/A snv 0.44 0.800 1.000 1 2011 2011
dbSNP: rs4143832
rs4143832
4 0.925 0.080 5 132527285 intron variant T/G snv 0.76 0.800 1.000 1 2009 2009
dbSNP: rs4857855
rs4857855
1 3 128541707 downstream gene variant C/T snv 0.18 0.800 1.000 1 2009 2009
dbSNP: rs9373124
rs9373124
3 6 135102071 intron variant T/C snv 0.33 0.800 1.000 1 2011 2011
dbSNP: rs1000005
rs1000005
1 21 33060745 intron variant G/C snv 0.51 0.700 1.000 1 2016 2016
dbSNP: rs10045577
rs10045577
1 5 111090753 intron variant C/A;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1004870
rs1004870
1 1 41905116 intron variant C/T snv 0.57 0.700 1.000 1 2019 2019
dbSNP: rs10075801
rs10075801
5 5 132341949 intron variant A/G snv 0.31 0.700 1.000 1 2016 2016
dbSNP: rs10083558
rs10083558
1 15 90659273 intron variant C/A snv 0.30 0.700 1.000 1 2019 2019
dbSNP: rs10118552
rs10118552
1 9 90004338 intron variant A/G snv 0.59 0.700 1.000 1 2019 2019
dbSNP: rs10135205
rs10135205
1 14 103316504 regulatory region variant A/G snv 0.54 0.700 1.000 1 2019 2019
dbSNP: rs10138752
rs10138752
5 14 68713254 intron variant C/T snv 8.8E-02 0.700 1.000 1 2016 2016
dbSNP: rs1013910
rs1013910
1 1 116868761 intergenic variant G/A snv 0.91 0.700 1.000 1 2019 2019
dbSNP: rs10147992
rs10147992
3 14 25034593 intron variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs10165200
rs10165200
2 2 8299499 intron variant G/A snv 0.36 0.700 1.000 1 2016 2016
dbSNP: rs10173538
rs10173538
5 2 159712765 intron variant C/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs10174238
rs10174238
14 0.724 0.200 2 191108308 intron variant G/A snv 0.70 0.700 1.000 1 2019 2019
dbSNP: rs10195713
rs10195713
1 2 157664393 intergenic variant C/T snv 0.89 0.700 1.000 1 2019 2019
dbSNP: rs10206089
rs10206089
4 2 61476184 intron variant G/A snv 0.700 1.000 1 2016 2016
dbSNP: rs10241173
rs10241173
1 7 124813204 intergenic variant A/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs1025687
rs1025687
3 18 50621423 intron variant T/C snv 0.61 0.700 1.000 1 2016 2016
dbSNP: rs10265538
rs10265538
2 7 20502242 intergenic variant T/C snv 0.20 0.700 1.000 1 2016 2016