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: rs13702
rs13702
LPL
7 0.925 0.160 8 19966981 3 prime UTR variant T/A;C snv 0.800 1.000 3 2011 2018
dbSNP: rs11570892
rs11570892
LPL
3 8 19966106 3 prime UTR variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs258
rs258
LPL
4 8 19954741 intron variant G/A;C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs271
rs271
LPL
4 1.000 0.040 8 19956191 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs28645722
rs28645722
LPL
3 8 19945383 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs287
rs287
LPL
3 8 19958045 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs316
rs316
LPL
3 8 19960925 missense variant C/A;T snv 0.13; 4.0E-06 0.700 1.000 1 2012 2012
dbSNP: rs320
rs320
LPL
9 0.827 0.200 8 19961566 intron variant T/A;G snv 0.700 1.000 1 2012 2012
dbSNP: rs3200218
rs3200218
LPL
3 8 19966560 3 prime UTR variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs9644636
rs9644636
LPL
3 8 19967385 downstream gene variant T/A;G snv 0.700 1.000 1 2012 2012
dbSNP: rs268
rs268
LPL
41 0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 0.800 1.000 4 2012 2019
dbSNP: rs3289
rs3289
LPL
3 8 19965681 3 prime UTR variant T/C snv 4.0E-02 0.800 1.000 2 2012 2019
dbSNP: rs1470186
rs1470186
LPL
3 8 19938278 intron variant T/C snv 6.6E-02 0.700 1.000 1 2012 2012
dbSNP: rs17091742
rs17091742
LPL
3 8 19938619 intron variant C/T snv 6.8E-02 0.700 1.000 1 2012 2012
dbSNP: rs28445964
rs28445964
LPL
3 8 19947085 intron variant A/G snv 7.0E-02 0.700 1.000 1 2012 2012
dbSNP: rs28575919
rs28575919
LPL
3 8 19945458 intron variant C/G snv 7.7E-02 0.700 1.000 1 2012 2012
dbSNP: rs6999612
rs6999612
LPL
3 8 19945573 intron variant T/C snv 7.8E-02 0.700 1.000 1 2012 2012
dbSNP: rs7000460
rs7000460
LPL
3 8 19946291 intron variant A/C snv 7.9E-02 0.700 1.000 1 2012 2012
dbSNP: rs343
rs343
LPL
4 1.000 0.080 8 19953276 intron variant C/A snv 9.8E-02 8.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs7016529
rs7016529
LPL
3 8 19949120 intron variant T/C snv 8.4E-02 0.800 1.000 2 2012 2018
dbSNP: rs328
rs328
LPL
19 0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02 0.800 1.000 8 2007 2019
dbSNP: rs325
rs325
LPL
4 8 19961817 intron variant T/C snv 9.0E-02 0.800 1.000 3 2008 2019
dbSNP: rs3735964
rs3735964
LPL
5 1.000 0.080 8 19966534 3 prime UTR variant C/A snv 9.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs28615996
rs28615996
LPL
3 8 19945200 intron variant T/C snv 9.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs11570891
rs11570891
LPL
2 8 19965299 intron variant C/T snv 9.5E-02; 2.1E-04 9.4E-02 0.700 1.000 1 2019 2019