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: rs3849942
rs3849942
9 0.776 0.200 9 27543283 non coding transcript exon variant T/A;C snv 0.870 1.000 8 2009 2018
dbSNP: rs2814707
rs2814707
4 0.882 0.120 9 27536399 non coding transcript exon variant C/G;T snv 0.830 1.000 6 2009 2014
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: rs13048019
rs13048019
1 1.000 0.080 21 31545981 intron variant C/T snv 0.14 0.810 1.000 2 2010 2014
dbSNP: rs4363506
rs4363506
1 1.000 0.080 10 127476239 intergenic variant T/C snv 0.41 0.810 1.000 2 2007 2009
dbSNP: rs7477
rs7477
1 1.000 0.080 17 16342702 3 prime UTR variant A/C snv 0.38 0.810 1.000 2 2013 2014
dbSNP: rs3113494
rs3113494
1 1.000 0.080 4 86911448 intron variant G/A snv 0.40 0.810 1.000 1 2012 2012
dbSNP: rs6703183
rs6703183
2 0.925 0.080 1 209539544 intron variant T/C snv 0.48 0.810 1.000 1 2013 2013
dbSNP: rs8141797
rs8141797
3 0.882 0.120 22 24186073 missense variant A/G snv 8.1E-02 9.8E-02 0.810 1.000 1 2013 2013
dbSNP: rs10122902
rs10122902
1 1.000 0.080 9 27556782 synonymous variant G/A snv 0.24 0.21 0.800 1.000 1 2010 2010
dbSNP: rs10438933
rs10438933
1 1.000 0.080 18 31693166 intergenic variant A/G snv 0.14 0.800 1.000 1 2009 2009
dbSNP: rs11082762
rs11082762
1 1.000 0.080 18 23785889 intron variant A/G;T snv 0.800 1.000 1 2013 2013
dbSNP: rs1971791
rs1971791
1 1.000 0.080 15 70283799 intergenic variant G/A snv 0.45 0.800 1.000 1 2013 2013
dbSNP: rs2006933
rs2006933
1 1.000 0.080 17 28274107 upstream gene variant T/G snv 0.23 0.800 1.000 1 2013 2013
dbSNP: rs2303565
rs2303565
1 1.000 0.080 2 218680586 intron variant T/C snv 0.43 0.56 0.800 1.000 1 2013 2013
dbSNP: rs5937496
rs5937496
1 1.000 0.080 X 76127599 regulatory region variant G/A snv 0.16 0.800 1.000 1 2009 2009
dbSNP: rs7577894
rs7577894
1 1.000 0.080 2 55781769 regulatory region variant T/C;G snv 0.800 1.000 1 2009 2009
dbSNP: rs8056742
rs8056742
1 1.000 0.080 16 85059142 intron variant T/C snv 0.22 0.800 1.000 1 2013 2013
dbSNP: rs855913
rs855913
1 1.000 0.080 7 149506571 intergenic variant A/C snv 0.96 0.800 1.000 1 2009 2009
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: rs10463311
rs10463311
1 1.000 0.080 5 151031274 intron variant C/T snv 0.66 0.710 1.000 2 2017 2018
dbSNP: rs903603
rs903603
1 1.000 0.080 9 27529318 non coding transcript exon variant G/A snv 0.39 0.710 1.000 2 2010 2013
dbSNP: rs3849943
rs3849943
5 0.827 0.080 9 27543384 non coding transcript exon variant C/G;T snv 0.700 1.000 3 2014 2018