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: rs12608932
rs12608932
5 0.827 0.080 19 17641880 intron variant A/C snv 0.36 0.880 0.923 13 2009 2019
dbSNP: rs2275294
rs2275294
3 0.925 0.080 20 63962894 intron variant G/A snv 0.25 0.060 0.833 6 2011 2018
dbSNP: rs10139154
rs10139154
2 0.925 0.120 14 30678292 intron variant C/T snv 0.46 0.720 0.750 4 2016 2019
dbSNP: rs1541160
rs1541160
3 0.882 0.080 1 170026661 intron variant C/A;T snv 0.830 1.000 4 2009 2014
dbSNP: rs10260404
rs10260404
2 0.925 0.080 7 154513713 intron variant T/C snv 0.35 0.820 0.667 3 2008 2011
dbSNP: rs10463311
rs10463311
1 1.000 0.080 5 151031274 intron variant C/T snv 0.66 0.710 1.000 2 2017 2018
dbSNP: rs13048019
rs13048019
1 1.000 0.080 21 31545981 intron variant C/T snv 0.14 0.810 1.000 2 2010 2014
dbSNP: rs7046653
rs7046653
1 1.000 0.080 9 27490969 intron variant A/G;T snv 0.700 1.000 2 2010 2013
dbSNP: rs74654358
rs74654358
1 1.000 0.080 12 64488187 intron variant G/A snv 3.0E-02 0.700 1.000 2 2016 2018
dbSNP: rs876016
rs876016
2 0.925 0.080 17 81852587 intron variant A/G snv 0.23 0.020 1.000 2 2013 2016
dbSNP: rs1008459
rs1008459
1 1.000 0.080 1 175182047 intron variant T/C snv 0.25 0.700 1.000 1 2007 2007
dbSNP: rs10143310
rs10143310
1 1.000 0.080 14 92074037 intron variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs10511816
rs10511816
1 1.000 0.080 9 27468463 intron variant C/A snv 0.30 0.700 1.000 1 2013 2013
dbSNP: rs10757665
rs10757665
1 1.000 0.080 9 27557921 intron variant T/C snv 0.20 0.700 1.000 1 2013 2013
dbSNP: rs10812605
rs10812605
1 1.000 0.080 9 27510362 intron variant C/T snv 0.58 0.700 1.000 1 2013 2013
dbSNP: rs10967952
rs10967952
1 1.000 0.080 9 27474216 intron variant T/C snv 0.17 0.700 1.000 1 2013 2013
dbSNP: rs10967958
rs10967958
1 1.000 0.080 9 27481907 intron variant C/T snv 0.13 0.700 1.000 1 2013 2013
dbSNP: rs10967959
rs10967959
1 1.000 0.080 9 27482969 intron variant C/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs10967976
rs10967976
1 1.000 0.080 9 27544945 intron variant G/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs11082762
rs11082762
1 1.000 0.080 18 23785889 intron variant A/G;T snv 0.800 1.000 1 2013 2013
dbSNP: rs11792285
rs11792285
1 1.000 0.080 9 27519175 intron variant C/T snv 0.28 0.700 1.000 1 2013 2013
dbSNP: rs11981433
rs11981433
4 0.882 0.240 7 95425028 intron variant T/C;G snv 0.010 1.000 1 2009 2009
dbSNP: rs12136973
rs12136973
3 1.000 0.080 1 175171183 intron variant T/C snv 0.22 0.700 1.000 1 2007 2007
dbSNP: rs12349820
rs12349820
1 1.000 0.080 9 27553878 intron variant T/C snv 0.20 0.700 1.000 1 2013 2013
dbSNP: rs12546767
rs12546767
2 0.925 0.120 8 125070323 intron variant T/C;G snv 0.700 1.000 1 2014 2014