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: rs326
rs326
LPL
2 8 19961928 intron variant A/G snv 0.37 0.800 1.000 4 2008 2019
dbSNP: rs328
rs328
LPL
3 0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02 0.800 1.000 4 2007 2019
dbSNP: rs15285
rs15285
LPL
5 1.000 0.040 8 19967156 3 prime UTR variant C/T snv 0.36 0.800 1.000 3 2011 2019
dbSNP: rs13702
rs13702
LPL
2 0.925 0.160 8 19966981 3 prime UTR variant T/A;C snv 0.800 1.000 2 2011 2018
dbSNP: rs268
rs268
LPL
3 0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 0.800 1.000 2 2012 2019
dbSNP: rs325
rs325
LPL
2 8 19961817 intron variant T/C snv 9.0E-02 0.800 1.000 2 2008 2019
dbSNP: rs3289
rs3289
LPL
1 8 19965681 3 prime UTR variant T/C snv 4.0E-02 0.800 1.000 1 2012 2019
dbSNP: rs7016529
rs7016529
LPL
2 8 19949120 intron variant T/C snv 8.4E-02 0.800 1.000 1 2012 2018
dbSNP: rs1059611
rs1059611
LPL
2 8 19967052 3 prime UTR variant T/C snv 0.13 0.700 1.000 1 2018 2018
dbSNP: rs11570891
rs11570891
LPL
1 8 19965299 intron variant C/T snv 9.5E-02; 2.1E-04 9.4E-02 0.700 1.000 1 2019 2019
dbSNP: rs287
rs287
LPL
3 8 19958045 intron variant A/G;T snv 0.700 1.000 1 2019 2019