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: rs8038465
rs8038465
1 15 73685996 intron variant C/T snv 0.31 0.800 1.000 1 2011 2011
dbSNP: rs9296736
rs9296736
1 6 54059899 intron variant T/C snv 0.51 0.800 1.000 1 2011 2011
dbSNP: rs9913711
rs9913711
1 17 72102020 intron variant G/A;C snv 0.800 1.000 1 2011 2011
dbSNP: rs4820599
rs4820599
6 0.925 0.160 22 24594246 intron variant A/G snv 0.43 0.700 1.000 2 2008 2011
dbSNP: rs4835265
rs4835265
6 4 145900258 intron variant C/A snv 0.15 0.700 1.000 2 2011 2018
dbSNP: rs10458877
rs10458877
1 11 15919553 intron variant C/T snv 0.18 0.700 1.000 1 2019 2019
dbSNP: rs10460702
rs10460702
1 21 29182833 intron variant G/A snv 2.4E-02 0.700 1.000 1 2018 2018
dbSNP: rs10497655
rs10497655
2 1.000 0.040 2 184597314 intron variant T/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs10913568
rs10913568
1 1 178544276 intron variant C/T snv 0.40 0.700 1.000 1 2018 2018
dbSNP: rs10917347
rs10917347
1 1 23050048 intron variant T/G snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs10919882
rs10919882
1 1 200291886 intron variant C/A snv 7.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs11002319
rs11002319
1 10 77876403 intron variant C/T snv 0.28 0.700 1.000 1 2018 2018
dbSNP: rs11066453
rs11066453
4 1.000 0.080 12 112927816 intron variant A/G snv 3.8E-03 0.700 1.000 1 2011 2011
dbSNP: rs111804060
rs111804060
1 1 154114036 intron variant G/A snv 0.28 0.700 1.000 1 2018 2018
dbSNP: rs1126617
rs1126617
1 6 24489424 missense variant C/T snv 0.29 0.31 0.700 1.000 1 2011 2011
dbSNP: rs115231893
rs115231893
1 22 24688848 downstream gene variant G/A snv 2.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs1169313
rs1169313
6 12 121004867 intron variant T/A;C snv 0.700 1.000 1 2008 2008
dbSNP: rs117322666
rs117322666
1 9 19586969 intron variant T/G snv 1.3E-02 0.700 1.000 1 2019 2019
dbSNP: rs117791138
rs117791138
1 12 24965415 downstream gene variant A/G snv 2.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs11830764
rs11830764
1 12 111077216 intron variant G/A;C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs12229654
rs12229654
20 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 0.700 1.000 1 2011 2011
dbSNP: rs12539316
rs12539316
6 0.925 0.120 7 73563568 downstream gene variant A/G snv 0.28 0.700 1.000 1 2011 2011
dbSNP: rs12594627
rs12594627
1 15 73693923 intron variant G/T snv 0.35 0.700 1.000 1 2018 2018
dbSNP: rs13084607
rs13084607
1 3 35736301 intron variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs13289095
rs13289095
1 9 128704210 intron variant G/T snv 0.12 0.700 1.000 1 2018 2018