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: rs12721054
rs12721054
3 19 44919330 3 prime UTR variant A/G snv 3.7E-02 0.800 1.000 6 2012 2019
dbSNP: rs2068888
rs2068888
5 10 93079885 downstream gene variant G/A snv 0.42 0.800 1.000 6 2010 2019
dbSNP: rs1077835
rs1077835
5 15 58431227 intron variant A/G snv 0.34 0.700 1.000 5 2015 2019
dbSNP: rs2131925
rs2131925
6 1 62560271 intron variant G/T snv 0.57 0.800 1.000 5 2010 2019
dbSNP: rs28927680
rs28927680
4 11 116748357 3 prime UTR variant C/G;T snv 0.800 1.000 5 2008 2019
dbSNP: rs2929282
rs2929282
2 15 43953733 intron variant A/T snv 0.13 0.800 1.000 5 2010 2019
dbSNP: rs326
rs326
LPL
4 8 19961928 intron variant A/G snv 0.37 0.800 1.000 5 2008 2019
dbSNP: rs442177
rs442177
5 4 87109109 intron variant G/T snv 0.56 0.800 1.000 5 2010 2019
dbSNP: rs9804646
rs9804646
3 11 116794363 upstream gene variant C/T snv 0.17 0.800 1.000 5 2012 2019
dbSNP: rs10761731
rs10761731
6 10 63267850 intron variant A/T snv 0.38 0.800 1.000 4 2010 2019
dbSNP: rs10808546
rs10808546
7 8 125483576 intron variant C/T snv 0.39 0.800 1.000 4 2012 2019
dbSNP: rs115849089
rs115849089
7 8 20054859 intergenic variant G/A snv 9.8E-02 0.700 1.000 4 2015 2019
dbSNP: rs174551
rs174551
6 11 61806212 5 prime UTR variant T/C snv 0.28 0.700 1.000 4 2018 2019
dbSNP: rs2238675
rs2238675
4 19 19225799 intron variant C/T snv 9.4E-02 0.800 1.000 4 2009 2019
dbSNP: rs2954022
rs2954022
4 8 125470379 intron variant C/A;T snv 0.700 1.000 4 2017 2019
dbSNP: rs2954031
rs2954031
9 8 125479491 intron variant G/T snv 0.42 0.800 1.000 4 2012 2019
dbSNP: rs2980875
rs2980875
6 8 125469505 intron variant A/C;G;T snv 0.800 1.000 4 2012 2019
dbSNP: rs35120633
rs35120633
1 11 116784884 missense variant G/A;C snv 6.6E-02; 8.0E-06 0.800 1.000 4 2009 2019
dbSNP: rs3741298
rs3741298
5 11 116786845 intron variant C/T snv 0.73 0.800 1.000 4 2012 2019
dbSNP: rs508487
rs508487
4 11 117204850 3 prime UTR variant C/T snv 5.2E-02 0.700 1.000 4 2011 2019
dbSNP: rs55707100
rs55707100
3 15 43528519 missense variant C/T snv 2.2E-02 2.0E-02 0.700 1.000 4 2014 2019
dbSNP: rs6065906
rs6065906
6 20 45925376 downstream gene variant T/A;C;G snv 0.800 1.000 4 2010 2019
dbSNP: rs10889353
rs10889353
5 1 62652525 intron variant A/C;T snv 0.800 1.000 3 2009 2019
dbSNP: rs1167998
rs1167998
6 1 62465961 intron variant C/A snv 0.57 0.800 1.000 3 2009 2019
dbSNP: rs13108218
rs13108218
7 4 3442204 intron variant A/G;T snv 0.700 1.000 3 2018 2019