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: rs369947678
rs369947678
2 0.925 0.080 X 56565446 missense variant C/A;G;T snv 2.0E-05; 2.7E-05; 3.3E-04 0.700 0
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: 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: rs10812611
rs10812611
1 1.000 0.080 9 27542263 non coding transcript exon variant C/T snv 0.42 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: rs11224052
rs11224052
1 1.000 0.080 11 134870879 intergenic variant G/A;T snv 0.27 0.700 1.000 1 2016 2016