Gene: LPL ×
Source: ALL
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
4 8 19961928 intron variant A/G snv 0.37 0.800 1.000 5 2008 2019
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: 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: rs264
rs264
LPL
6 0.882 0.080 8 19955669 intron variant G/A snv 0.14 0.700 1.000 3 2009 2013
dbSNP: rs325
rs325
LPL
4 8 19961817 intron variant T/C snv 9.0E-02 0.800 1.000 3 2008 2019
dbSNP: rs12679834
rs12679834
LPL
7 8 19962922 intron variant T/C snv 9.4E-02 0.700 1.000 2 2012 2012
dbSNP: rs327
rs327
LPL
4 8 19962025 intron variant T/G snv 0.31 0.700 1.000 2 2012 2012
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: rs3916027
rs3916027
LPL
3 8 19967357 downstream gene variant G/A snv 0.31 0.700 1.000 2 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: rs1031045
rs1031045
LPL
3 8 19943601 intron variant G/A snv 0.12 0.700 1.000 1 2012 2012
dbSNP: rs1059507
rs1059507
LPL
4 1.000 0.080 8 19966452 3 prime UTR variant C/T snv 0.15 0.700 1.000 1 2012 2012
dbSNP: rs1059611
rs1059611
LPL
3 8 19967052 3 prime UTR variant T/C snv 0.13 0.700 1.000 1 2018 2018
dbSNP: rs11570892
rs11570892
LPL
3 8 19966106 3 prime UTR variant A/G;T snv 0.700 1.000 1 2012 2012
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: rs1800590
rs1800590
LPL
3 8 19939160 intron variant T/G snv 0.13 0.700 1.000 1 2012 2012
dbSNP: rs253
rs253
LPL
4 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: rs258
rs258
LPL
4 8 19954741 intron variant G/A;C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs263
rs263
LPL
4 1.000 0.040 8 19955301 intron variant C/T snv 0.23 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: rs28445964
rs28445964
LPL
3 8 19947085 intron variant A/G snv 7.0E-02 0.700 1.000 1 2012 2012
dbSNP: rs285
rs285
LPL
5 1.000 0.080 8 19957678 intron variant C/T snv 0.59 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