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: rs301
rs301
LPL
7 0.925 0.160 8 19959423 intron variant T/C snv 0.24 0.26 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: 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: rs3208305
rs3208305
LPL
4 1.000 0.080 8 19966137 3 prime UTR variant A/T snv 0.36 0.700 1.000 1 2012 2012
dbSNP: rs325
rs325
LPL
4 8 19961817 intron variant T/C snv 9.0E-02 0.800 1.000 3 2008 2019
dbSNP: rs326
rs326
LPL
4 8 19961928 intron variant A/G snv 0.37 0.800 1.000 5 2008 2019
dbSNP: rs327
rs327
LPL
4 8 19962025 intron variant T/G snv 0.31 0.700 1.000 2 2012 2012
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: rs3289
rs3289
LPL
3 8 19965681 3 prime UTR variant T/C snv 4.0E-02 0.800 1.000 2 2012 2019
dbSNP: rs331
rs331
LPL
4 8 19962894 intron variant G/A snv 0.30 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: 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: rs3779788
rs3779788
LPL
3 8 19945582 intron variant C/T snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs3916027
rs3916027
LPL
3 8 19967357 downstream gene variant G/A snv 0.31 0.700 1.000 2 2012 2012
dbSNP: rs4921683
rs4921683
LPL
3 8 19967557 downstream gene variant T/A snv 0.14 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
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: rs7009128
rs7009128
LPL
3 8 19930017 intron variant T/C snv 0.10 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: rs9644636
rs9644636
LPL
3 8 19967385 downstream gene variant T/A;G snv 0.700 1.000 1 2012 2012