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: rs7000460
rs7000460
LPL
3 8 19946291 intron variant A/C snv 7.9E-02 0.700 1.000 1 2012 2012
dbSNP: rs268
rs268
LPL
4 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: rs326
rs326
LPL
3 8 19961928 intron variant A/G snv 0.37 0.800 1.000 2 2008 2019
dbSNP: rs28445964
rs28445964
LPL
3 8 19947085 intron variant A/G snv 7.0E-02 0.700 1.000 1 2012 2012
dbSNP: rs11570892
rs11570892
LPL
3 8 19966106 3 prime UTR variant A/G;T 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: rs3208305
rs3208305
LPL
3 1.000 0.080 8 19966137 3 prime UTR variant A/T snv 0.36 0.700 1.000 1 2012 2012
dbSNP: rs343
rs343
LPL
3 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: rs3735964
rs3735964
LPL
4 1.000 0.080 8 19966534 3 prime UTR variant C/A snv 9.1E-02 0.700 1.000 1 2012 2012
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: rs328
rs328
LPL
7 0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02 0.800 1.000 6 2007 2019
dbSNP: rs28575919
rs28575919
LPL
3 8 19945458 intron variant C/G snv 7.7E-02 0.700 1.000 1 2012 2012
dbSNP: rs1059507
rs1059507
LPL
3 1.000 0.080 8 19966452 3 prime UTR variant C/T snv 0.15 0.700 1.000 1 2012 2012
dbSNP: rs15285
rs15285
LPL
1 1.000 0.040 8 19967156 3 prime UTR variant C/T snv 0.36 0.800 1.000 1 2011 2019
dbSNP: rs17091742
rs17091742
LPL
3 8 19938619 intron variant C/T snv 6.8E-02 0.700 1.000 1 2012 2012
dbSNP: rs253
rs253
LPL
3 1.000 0.040 8 19953906 intron variant C/T snv 0.53 0.700 1.000 1 2012 2012
dbSNP: rs256
rs256
LPL
3 8 19954456 intron variant C/T snv 0.12 0.700 1.000 1 2012 2012
dbSNP: rs263
rs263
LPL
3 1.000 0.040 8 19955301 intron variant C/T snv 0.23 0.700 1.000 1 2012 2012
dbSNP: rs285
rs285
LPL
3 1.000 0.080 8 19957678 intron variant C/T snv 0.59 0.700 1.000 1 2012 2012
dbSNP: rs3779788
rs3779788
LPL
3 8 19945582 intron variant C/T snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs264
rs264
LPL
4 0.882 0.080 8 19955669 intron variant G/A snv 0.14 0.700 1.000 3 2009 2013
dbSNP: rs3916027
rs3916027
LPL
3 8 19967357 downstream gene variant G/A snv 0.31 0.700 1.000 2 2012 2012
dbSNP: rs1031045
rs1031045
LPL
3 8 19943601 intron variant G/A snv 0.12 0.700 1.000 1 2012 2012
dbSNP: rs331
rs331
LPL
3 8 19962894 intron variant G/A snv 0.30 0.700 1.000 1 2012 2012
dbSNP: rs4922115
rs4922115
LPL
3 8 19965319 3 prime UTR variant G/A snv 0.15 0.14 0.700 1.000 1 2012 2012