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: rs1143678
rs1143678
1 1.000 0.080 16 31331684 missense variant C/T snv 0.15 0.17 0.730 1.000 6 2008 2017
dbSNP: rs1143683
rs1143683
1 1.000 0.080 16 31325567 missense variant C/T snv 0.16 0.16 0.730 1.000 4 2009 2013
dbSNP: rs10239340
rs10239340
1 1.000 0.080 7 129028456 intron variant T/A;G snv 0.700 1.000 3 2008 2014
dbSNP: rs12537284
rs12537284
1 1.000 0.080 7 129077852 intergenic variant G/A snv 0.11 0.800 1.000 3 2008 2014
dbSNP: rs13205210
rs13205210
1 1.000 0.080 6 34864079 missense variant T/C snv 0.11 0.13 0.720 1.000 3 2011 2019
dbSNP: rs1385374
rs1385374
1 1.000 0.080 12 128816149 intron variant C/T snv 9.1E-02 0.810 1.000 3 2009 2016
dbSNP: rs148833270
rs148833270
1 1.000 0.080 3 48467524 missense variant C/T snv 6.4E-05 2.1E-05 0.700 1.000 3 2007 2013
dbSNP: rs35000415
rs35000415
1 1.000 0.080 7 128945562 intron variant C/T snv 9.0E-02 0.700 1.000 3 2015 2017
dbSNP: rs3757173
rs3757173
1 1.000 0.080 6 137869017 intron variant A/G snv 0.20 0.720 1.000 3 2012 2016
dbSNP: rs387619
rs387619
1 1.000 0.080 11 35076646 intergenic variant T/A;C snv 0.710 1.000 3 2011 2016
dbSNP: rs72556555
rs72556555
1 1.000 0.080 3 48467375 missense variant G/A;C snv 2.0E-05; 2.0E-04 0.700 1.000 3 2007 2013
dbSNP: rs7444
rs7444
2 1.000 0.080 22 21622645 3 prime UTR variant T/C snv 0.32 0.700 1.000 3 2015 2017
dbSNP: rs762011967
rs762011967
1 1.000 0.080 3 48467128 missense variant C/T snv 4.4E-05 4.2E-05 0.700 1.000 3 2007 2013
dbSNP: rs7726414
rs7726414
1 1.000 0.080 5 134096143 intergenic variant C/T snv 0.15 0.710 1.000 3 2015 2017
dbSNP: rs9462027
rs9462027
1 1.000 0.080 6 34829464 intron variant G/A snv 0.37 0.700 1.000 3 2015 2017
dbSNP: rs9652601
rs9652601
1 1.000 0.080 16 11080508 intron variant G/A snv 0.34 0.700 1.000 3 2015 2017
dbSNP: rs10048743
rs10048743
1 1.000 0.080 2 213025508 intron variant G/T snv 0.78 0.700 1.000 2 2015 2016
dbSNP: rs1059312
rs1059312
1 1.000 0.080 12 128794319 synonymous variant A/G snv 0.44 0.43 0.700 1.000 2 2015 2017
dbSNP: rs10912578
rs10912578
1 1.000 0.080 1 173282717 intergenic variant A/G snv 0.63 0.700 1.000 2 2015 2016
dbSNP: rs11644034
rs11644034
1 1.000 0.080 16 85939006 intron variant G/A snv 0.19 0.710 0.500 2 2014 2015
dbSNP: rs11755393
rs11755393
2 1.000 0.080 6 34856859 missense variant A/G;T snv 0.36 0.710 1.000 2 2009 2011
dbSNP: rs13239597
rs13239597
3 0.882 0.080 7 129055929 non coding transcript exon variant C/A snv 9.0E-02 0.710 1.000 2 2013 2020
dbSNP: rs13306575
rs13306575
1 1.000 0.080 1 183563302 missense variant G/A;C;T snv 1.9E-02; 4.0E-06; 4.0E-06 0.710 1.000 2 2015 2016
dbSNP: rs13332649
rs13332649
1 1.000 0.080 16 85933077 intron variant A/G snv 0.18 0.700 1.000 2 2015 2016
dbSNP: rs1370031102
rs1370031102
1 1.000 0.080 4 87982700 missense variant C/T snv 4.0E-06 7.0E-06 0.020 0.500 2 2002 2017