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: rs920778
rs920778
36 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.030 1.000 3 2017 2019
dbSNP: rs965513
rs965513
15 0.742 0.200 9 97793827 intron variant A/G;T snv 0.020 1.000 2 2014 2019
dbSNP: rs966423
rs966423
11 0.776 0.200 2 217445617 intron variant C/G;T snv 0.020 1.000 2 2016 2019
dbSNP: rs10053538
rs10053538
7 0.807 0.160 5 157110499 intron variant C/A;T snv 0.010 1.000 1 2016 2016
dbSNP: rs10505477
rs10505477
31 0.658 0.400 8 127395198 intron variant A/G snv 0.40 0.010 1.000 1 2015 2015
dbSNP: rs11225395
rs11225395
11 0.776 0.360 11 102725749 intron variant A/C;G snv 0.010 1.000 1 2007 2007
dbSNP: rs1143630
rs1143630
5 0.827 0.160 2 112834078 intron variant T/A;G snv 0.010 1.000 1 2012 2012
dbSNP: rs1143633
rs1143633
11 0.752 0.280 2 112832890 intron variant C/G;T snv 0.010 1.000 1 2012 2012
dbSNP: rs1143643
rs1143643
10 0.790 0.320 2 112830725 intron variant C/T snv 0.29 0.010 1.000 1 2012 2012
dbSNP: rs11581557
rs11581557
1 1.000 0.080 1 39862786 intron variant A/C;T snv 0.010 1.000 1 2013 2013
dbSNP: rs11600655
rs11600655
2 0.925 0.120 11 63606853 intron variant G/C snv 0.27 0.010 1.000 1 2019 2019
dbSNP: rs11886868
rs11886868
12 0.752 0.280 2 60493111 intron variant C/T snv 0.65 0.010 1.000 1 2017 2017
dbSNP: rs1190271
rs1190271
1 1.000 0.080 6 105176946 intron variant G/A;C snv 0.010 1.000 1 2012 2012
dbSNP: rs1219648
rs1219648
17 0.716 0.320 10 121586676 intron variant A/G;T snv 0.010 1.000 1 2011 2011
dbSNP: rs13042395
rs13042395
13 0.752 0.160 20 773867 intron variant C/T snv 5.9E-02 0.010 1.000 1 2016 2016
dbSNP: rs13140012
rs13140012
6 0.827 0.320 4 186544404 intron variant T/A snv 0.41 0.010 1.000 1 2015 2015
dbSNP: rs13293512
rs13293512
11 0.763 0.360 9 94167461 intron variant T/C snv 0.24 0.010 1.000 1 2015 2015
dbSNP: rs16893344
rs16893344
7 0.807 0.160 8 133194036 intron variant C/T snv 0.29 0.010 1.000 1 2017 2017
dbSNP: rs187115
rs187115
22 0.695 0.320 11 35154612 intron variant T/C snv 0.37 0.010 1.000 1 2019 2019
dbSNP: rs2064863
rs2064863
4 0.925 0.120 20 56387716 intron variant T/A;C;G snv 0.010 1.000 1 2019 2019
dbSNP: rs2070744
rs2070744
54 0.608 0.680 7 150992991 intron variant C/T snv 0.70 0.010 1.000 1 2019 2019
dbSNP: rs2105269
rs2105269
4 0.882 0.120 14 69280517 intron variant A/G snv 0.35 0.010 1.000 1 2019 2019
dbSNP: rs2253319
rs2253319
3 0.882 0.120 21 34815749 intron variant C/G;T snv 0.010 1.000 1 2011 2011
dbSNP: rs243865
rs243865
48 0.600 0.640 16 55477894 intron variant C/T snv 0.19 0.010 1.000 1 2011 2011
dbSNP: rs2439302
rs2439302
9 0.776 0.200 8 32574851 intron variant G/C snv 0.54 0.010 1.000 1 2016 2016