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: rs10231372
rs10231372
1 7 150435975 intron variant T/C snv 0.67 0.700 1.000 1 2018 2018
dbSNP: rs112196420
rs112196420
1 3 69450652 intron variant G/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs115842101
rs115842101
1 3 72539980 intron variant C/T snv 3.7E-02 0.700 1.000 1 2019 2019
dbSNP: rs1159970
rs1159970
1 1 233156205 intron variant C/T snv 0.34 0.700 1.000 1 2018 2018
dbSNP: rs11677128
rs11677128
1 2 234745466 non coding transcript exon variant T/C snv 0.44 0.700 1.000 1 2018 2018
dbSNP: rs11720469
rs11720469
1 3 166763420 intergenic variant G/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs12068986
rs12068986
1 1 158121627 regulatory region variant C/T snv 0.29 0.700 1.000 1 2014 2014
dbSNP: rs13163913
rs13163913
1 5 99970233 intergenic variant T/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs13247707
rs13247707
1 7 11779851 intron variant T/C snv 0.25 0.700 1.000 1 2019 2019
dbSNP: rs1687482
rs1687482
1 3 126496851 intron variant T/G snv 0.72 0.700 1.000 1 2017 2017
dbSNP: rs17055223
rs17055223
1 6 128023640 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs17432268
rs17432268
1 7 18446819 intron variant A/G snv 6.0E-03 0.700 1.000 1 2019 2019
dbSNP: rs2252790
rs2252790
DSE
1 6 116342160 intron variant G/A snv 0.76 0.700 1.000 1 2017 2017
dbSNP: rs258430
rs258430
1 12 27880569 intergenic variant A/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs28364570
rs28364570
1 14 22815695 5 prime UTR variant A/G snv 0.11 0.17 0.700 1.000 1 2019 2019
dbSNP: rs372255102
rs372255102
1 21 26630728 intergenic variant T/C snv 5.2E-02 0.700 1.000 1 2017 2017
dbSNP: rs6544273
rs6544273
1 2 39952065 intron variant C/T snv 0.58 0.700 1.000 1 2019 2019
dbSNP: rs6867021
rs6867021
1 5 79933823 upstream gene variant A/G snv 0.64 0.700 1.000 1 2018 2018
dbSNP: rs7119037
rs7119037
1 11 20244845 intergenic variant C/A;G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs79472635
rs79472635
1 16 21140753 intron variant A/G snv 0.700 1.000 1 2019 2019
dbSNP: rs830142
rs830142
1 19 47446095 intron variant G/A snv 4.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs9478638
rs9478638
1 6 155327361 regulatory region variant G/A snv 0.27 0.700 1.000 1 2014 2014
dbSNP: rs9514041
rs9514041
1 13 102690290 intron variant G/A snv 0.12 0.700 1.000 1 2018 2018
dbSNP: rs984924
rs984924
1 4 81199758 intron variant A/G snv 0.20 0.700 1.000 1 2018 2018