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: rs28374715
rs28374715
1 1.000 0.040 15 41271752 intron variant A/G snv 0.25 0.800 1.000 3 2012 2017
dbSNP: rs11739663
rs11739663
1 1.000 0.040 5 593968 intergenic variant T/C snv 0.29 0.800 1.000 2 2011 2012
dbSNP: rs4598195
rs4598195
1 1.000 0.040 7 107862996 intergenic variant A/C snv 0.34 0.800 1.000 2 2009 2010
dbSNP: rs6088765
rs6088765
1 1.000 0.040 20 35211477 intron variant T/G snv 0.54 0.800 1.000 2 2012 2015
dbSNP: rs886774
rs886774
1 1.000 0.040 7 107854989 regulatory region variant G/A snv 0.67 0.810 1.000 2 2009 2015
dbSNP: rs10035653
rs10035653
1 1.000 0.040 5 442675 non coding transcript exon variant G/A;T snv 9.1E-02; 4.0E-06 0.010 1.000 1 2018 2018
dbSNP: rs1016883
rs1016883
1 1.000 0.040 2 198016944 intron variant G/A snv 0.20 0.800 1.000 1 2012 2012
dbSNP: rs10415946
rs10415946
1 1.000 0.040 19 41755151 intron variant A/G snv 0.39 0.010 1.000 1 2011 2011
dbSNP: rs10416839
rs10416839
1 1.000 0.040 19 41776424 intron variant G/T snv 0.26 0.010 1.000 1 2011 2011
dbSNP: rs10910092
rs10910092
1 1.000 0.040 1 2570077 downstream gene variant A/G snv 0.52 0.700 1.000 1 2015 2015
dbSNP: rs11054935
rs11054935
1 1.000 0.040 12 12495909 intron variant A/G snv 0.22 0.700 1.000 1 2015 2015
dbSNP: rs11083840
rs11083840
1 1.000 0.040 19 46616653 downstream gene variant T/G snv 0.44 0.700 1.000 1 2015 2015
dbSNP: rs11133504
rs11133504
1 1.000 0.040 4 57514156 intergenic variant G/A snv 0.23 0.700 1.000 1 2014 2014
dbSNP: rs1126510
rs1126510
1 1.000 0.040 19 46620526 3 prime UTR variant A/G snv 0.31 0.800 1.000 1 2012 2012
dbSNP: rs113986290
rs113986290
1 1.000 0.040 6 19780778 intron variant C/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs11583043
rs11583043
1 1.000 0.040 1 101000498 intron variant C/T snv 0.28 0.700 1.000 1 2015 2015
dbSNP: rs12149608
rs12149608
1 1.000 0.040 16 68552601 intron variant G/C snv 6.5E-02 0.700 1.000 1 2015 2015
dbSNP: rs12261843
rs12261843
1 1.000 0.040 10 35265126 intron variant T/C;G snv 0.800 1.000 1 2011 2011
dbSNP: rs13337840
rs13337840
1 1.000 0.040 16 86793733 intergenic variant A/G snv 0.28 0.700 1.000 1 2009 2009
dbSNP: rs1336123245
rs1336123245
1 1.000 0.040 1 74710189 missense variant G/A snv 4.0E-06 0.010 1.000 1 2009 2009
dbSNP: rs13381619
rs13381619
1 1.000 0.040 18 47890513 intron variant C/G snv 0.22 0.010 1.000 1 2019 2019
dbSNP: rs138788
rs138788
1 1.000 0.040 22 35333728 intron variant G/A snv 0.49 0.700 1.000 1 2017 2017
dbSNP: rs140797839
rs140797839
1 1.000 0.040 19 54933725 missense variant C/T snv 4.8E-05 6.3E-05 0.010 1.000 1 2018 2018
dbSNP: rs143169084
rs143169084
1 1.000 0.040 19 54939737 missense variant G/A snv 2.0E-03 1.2E-03 0.010 1.000 1 2018 2018
dbSNP: rs1440088
rs1440088
1 1.000 0.040 2 198006693 intron variant T/G snv 0.21 0.700 1.000 1 2015 2015