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: rs6993770
rs6993770
9 0.925 0.080 8 105569300 intron variant A/T snv 0.31 0.800 1.000 2 2011 2016
dbSNP: rs10738760
rs10738760
7 0.807 0.320 9 2691186 regulatory region variant A/G snv 0.56 0.800 1.000 1 2011 2011
dbSNP: rs4513773
rs4513773
1 6 43957789 intergenic variant A/G snv 0.44 0.800 1.000 1 2011 2011
dbSNP: rs9472155
rs9472155
1 6 43929990 intergenic variant C/T snv 0.28 0.800 1.000 1 2011 2011
dbSNP: rs6921438
rs6921438
10 0.776 0.360 6 43957870 intergenic variant G/A;C snv 0.700 1.000 2 2016 2017
dbSNP: rs7030781
rs7030781
1 9 2686273 intergenic variant A/G;T snv 0.700 1.000 2 2017 2019
dbSNP: rs10122587
rs10122587
1 9 2691951 intergenic variant C/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs10761731
rs10761731
6 10 63267850 intron variant A/T snv 0.38 0.700 1.000 1 2017 2017
dbSNP: rs10761741
rs10761741
4 1.000 0.040 10 63306426 intron variant G/T snv 0.38 0.700 1.000 1 2016 2016
dbSNP: rs10761750
rs10761750
1 10 63368859 intron variant G/A snv 0.43 0.700 1.000 1 2017 2017
dbSNP: rs10967470
rs10967470
1 9 2675698 intergenic variant A/G snv 0.21 0.700 1.000 1 2011 2011
dbSNP: rs10967492
rs10967492
1 9 2681175 intergenic variant T/A snv 0.18 0.700 1.000 1 2011 2011
dbSNP: rs114694170
rs114694170
5 1.000 0.040 5 88884379 non coding transcript exon variant T/C snv 3.6E-02 0.700 1.000 1 2016 2016
dbSNP: rs12199215
rs12199215
2 6 44059177 non coding transcript exon variant C/T snv 0.25 0.700 1.000 1 2017 2017
dbSNP: rs12214617
rs12214617
1 6 43972186 intergenic variant G/T snv 0.53 0.700 1.000 1 2017 2017
dbSNP: rs1349319
rs1349319
1 8 105544406 intron variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs143479231
rs143479231
1 3 193393005 intergenic variant G/A snv 1.5E-02 0.700 1.000 1 2017 2017
dbSNP: rs144085478
rs144085478
1 6 44432305 intron variant T/C snv 8.9E-03 0.700 1.000 1 2017 2017
dbSNP: rs144820908
rs144820908
1 6 44545748 intergenic variant A/C snv 4.0E-03 0.700 1.000 1 2017 2017
dbSNP: rs16873291
rs16873291
1 8 105515802 intron variant C/T snv 0.40 0.700 1.000 1 2011 2011
dbSNP: rs16873365
rs16873365
1 8 105546007 intron variant C/T snv 0.11 0.700 1.000 1 2011 2011
dbSNP: rs16873402
rs16873402
1 8 105577019 intron variant C/T snv 0.40 0.700 1.000 1 2011 2011
dbSNP: rs1740073
rs1740073
2 1.000 0.040 6 43979661 regulatory region variant T/C snv 0.67 0.700 1.000 1 2016 2016
dbSNP: rs1776717
rs1776717
1 6 43983599 regulatory region variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs1776721
rs1776721
1 6 43923246 regulatory region variant G/A;T snv 0.700 1.000 1 2011 2011