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: rs10748781
rs10748781
11 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 0.700 1.000 1 2016 2016
dbSNP: rs10750899
rs10750899
5 0.827 0.120 11 58517478 intergenic variant G/A snv 0.95 0.700 1.000 1 2016 2016
dbSNP: rs10757278
rs10757278
44 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.010 1.000 1 2020 2020
dbSNP: rs10758669
rs10758669
10 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs10761648
rs10761648
5 0.827 0.120 10 62594503 intron variant C/T snv 0.20 0.700 1.000 1 2016 2016
dbSNP: rs10775412
rs10775412
5 0.827 0.120 17 27542007 intron variant A/C snv 0.30 0.700 1.000 1 2016 2016
dbSNP: rs10782001
rs10782001
2 1.000 0.040 16 30931304 intron variant G/A snv 0.53 0.800 1.000 2 2010 2015
dbSNP: rs10789229
rs10789229
1 1.000 0.040 1 67239891 intron variant C/T snv 0.62 0.010 1.000 1 2013 2013
dbSNP: rs10789285
rs10789285
2 1.000 0.040 1 69322799 intergenic variant T/G snv 0.33 0.700 1.000 1 2015 2015
dbSNP: rs10794648
rs10794648
1 1.000 0.040 1 24191716 upstream gene variant T/C snv 0.68 0.700 1.000 2 2015 2015
dbSNP: rs10800314
rs10800314
5 0.827 0.120 1 161502999 upstream gene variant C/A snv 0.65 0.700 1.000 1 2016 2016
dbSNP: rs10822050
rs10822050
14 0.724 0.240 10 62679011 downstream gene variant T/C snv 0.33 0.700 1.000 1 2015 2015
dbSNP: rs10852936
rs10852936
3 0.925 0.120 17 39875461 intron variant C/T snv 0.39 0.40 0.010 1.000 1 2014 2014
dbSNP: rs10865331
rs10865331
5 0.827 0.120 2 62324337 intergenic variant A/G snv 0.57 0.800 1.000 1 2012 2012
dbSNP: rs10870077
rs10870077
5 0.827 0.120 9 136369439 intron variant C/G snv 0.38 0.700 1.000 1 2016 2016
dbSNP: rs10888501
rs10888501
1 1.000 0.040 1 152565478 downstream gene variant G/A snv 0.48 0.700 1.000 1 2015 2015
dbSNP: rs10888503
rs10888503
2 0.925 0.080 1 152621073 downstream gene variant C/T snv 0.59 0.010 1.000 1 2015 2015
dbSNP: rs10889676
rs10889676
5 0.827 0.120 1 67256884 intron variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs10889677
rs10889677
40 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 0.010 < 0.001 1 2016 2016
dbSNP: rs10930046
rs10930046
3 0.882 0.200 2 162281473 missense variant T/C snv 9.7E-02 0.16 0.010 1.000 1 2010 2010
dbSNP: rs10960680
rs10960680
1 1.000 0.040 9 12483941 intergenic variant A/C snv 9.4E-02 0.700 1.000 1 2019 2019
dbSNP: rs10979182
rs10979182
1 1.000 0.040 9 108054739 regulatory region variant A/G snv 0.44 0.800 1.000 1 2012 2012
dbSNP: rs10988542
rs10988542
14 0.724 0.240 9 129894985 intron variant G/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs10995271
rs10995271
8 0.776 0.280 10 62678726 downstream gene variant G/C snv 0.32 0.700 1.000 1 2016 2016
dbSNP: rs11053802
rs11053802
1 1.000 0.040 12 10444608 intron variant C/G;T snv 0.700 1.000 1 2017 2017