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: rs9815354
rs9815354
4 0.925 0.160 3 41871159 intron variant G/A;T snv 0.700 1.000 3 2009 2017
dbSNP: rs1717027
rs1717027
3 1.000 0.160 3 41946428 intron variant T/A;C snv 0.700 1.000 2 2013 2019
dbSNP: rs114714860
rs114714860
1 3 41841413 intron variant G/C snv 0.33 0.700 1.000 1 2017 2017
dbSNP: rs147428270
rs147428270
1 3 41827229 intron variant T/C snv 0.27 0.700 1.000 1 2017 2017
dbSNP: rs1716983
rs1716983
3 1.000 0.160 3 41922636 intron variant G/A;C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs2683696
rs2683696
2 1.000 0.160 3 41873406 intron variant T/C snv 0.34 0.700 1.000 1 2019 2019
dbSNP: rs73081364
rs73081364
3 1.000 0.160 3 41872124 intron variant G/A;C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs7372217
rs7372217
4 1.000 0.160 3 41948630 intron variant G/A snv 0.68 0.700 1.000 1 2017 2017
dbSNP: rs7622665
rs7622665
3 1.000 0.160 3 41929251 intron variant T/C snv 0.67 0.700 1.000 1 2018 2018
dbSNP: rs7651190
rs7651190
4 1.000 0.160 3 41724463 intron variant A/G snv 0.33 0.700 1.000 1 2017 2017
dbSNP: rs79211428
rs79211428
2 3 41880318 intron variant C/T snv 0.19 0.700 1.000 1 2018 2018
dbSNP: rs2272007
rs2272007
2 1.000 0.160 3 41954644 missense variant T/C snv 0.79 0.67 0.700 1.000 2 2016 2016
dbSNP: rs3774372
rs3774372
4 1.000 0.160 3 41835922 missense variant T/C snv 0.17 0.18 0.700 1.000 1 2016 2016