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: rs218237
rs218237
6 4 54528005 intergenic variant C/T snv 0.18 0.800 1.000 5 2009 2019
dbSNP: rs218238
rs218238
3 4 54528857 intergenic variant A/T snv 0.38 0.800 1.000 4 2009 2018
dbSNP: rs10168349
rs10168349
4 2 46133768 intron variant G/C snv 0.36 0.700 1.000 3 2016 2019
dbSNP: rs1434282
rs1434282
6 1 199041592 non coding transcript exon variant C/T snv 0.76 0.700 1.000 3 2016 2019
dbSNP: rs1547247
rs1547247
5 6 135069698 intron variant G/A snv 0.22 0.800 1.000 3 2009 2019
dbSNP: rs2075672
rs2075672
8 7 100642673 intron variant A/G snv 0.65 0.700 1.000 3 2012 2017
dbSNP: rs3809627
rs3809627
5 16 30091839 5 prime UTR variant C/A snv 0.41 0.700 1.000 3 2016 2019
dbSNP: rs3811444
rs3811444
12 1 247876149 missense variant C/T snv 0.31 0.26 0.700 1.000 3 2012 2019
dbSNP: rs6569992
rs6569992
4 6 135131014 intergenic variant G/A;C;T snv 0.800 1.000 3 2009 2012
dbSNP: rs6592965
rs6592965
4 7 50360284 intron variant G/A snv 0.47 0.700 1.000 3 2016 2019
dbSNP: rs9349205
rs9349205
7 6 41957421 intron variant G/A;C snv 0.700 1.000 3 2016 2019
dbSNP: rs9573567
rs9573567
2 13 75483247 upstream gene variant G/A snv 6.8E-02 0.700 1.000 3 2016 2019
dbSNP: rs10758656
rs10758656
7 9 4852599 intron variant A/G snv 0.19 0.800 1.000 2 2009 2019
dbSNP: rs10758658
rs10758658
4 9 4856877 intron variant G/A snv 0.15 0.700 1.000 2 2017 2018
dbSNP: rs10947997
rs10947997
4 6 41953503 intron variant G/T snv 0.13 0.800 1.000 2 2009 2016
dbSNP: rs11072567
rs11072567
5 15 76006403 intron variant A/G snv 0.43 0.700 1.000 2 2016 2019
dbSNP: rs115986297
rs115986297
3 6 2050557 intron variant A/C;G snv 0.700 1.000 2 2016 2019
dbSNP: rs11628273
rs11628273
2 14 65043160 intron variant C/T snv 0.57 0.800 1.000 2 2009 2019
dbSNP: rs1175550
rs1175550
5 1 3774964 intron variant A/G snv 0.31 0.700 1.000 2 2016 2019
dbSNP: rs117747069
rs117747069
4 16 120077 intron variant G/C snv 2.5E-02 0.700 1.000 2 2016 2019
dbSNP: rs1256061
rs1256061
5 14 64236875 intron variant G/A;T snv 0.700 1.000 2 2016 2019
dbSNP: rs12903896
rs12903896
1 15 74760154 downstream gene variant C/T snv 0.43 0.700 1.000 2 2016 2019
dbSNP: rs1320963
rs1320963
5 6 135122074 intergenic variant A/G snv 0.35 0.700 1.000 2 2009 2012
dbSNP: rs13335629
rs13335629
4 16 260381 intron variant G/A;C snv 1.1E-02 0.700 1.000 2 2013 2017
dbSNP: rs143593369
rs143593369
1 7 100711557 downstream gene variant A/G snv 4.8E-03 0.700 1.000 2 2016 2019