Gene: LPL ×
Source: GWASDB ×
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: rs256
rs256
LPL
3 8 19954456 intron variant C/T snv 0.12 0.700 1.000 1 2012 2012
dbSNP: rs258
rs258
LPL
3 8 19954741 intron variant G/A;C;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: rs28575919
rs28575919
LPL
3 8 19945458 intron variant C/G snv 7.7E-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: rs28645722
rs28645722
LPL
3 8 19945383 intron variant G/A;T snv 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: rs3200218
rs3200218
LPL
3 8 19966560 3 prime UTR variant A/G;T snv 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 1 2008 2019
dbSNP: rs3289
rs3289
LPL
3 8 19965681 3 prime UTR variant T/C snv 4.0E-02 0.800 1.000 1 2012 2019
dbSNP: rs331
rs331
LPL
3 8 19962894 intron variant G/A snv 0.30 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: 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 1 2012 2018
dbSNP: rs9644636
rs9644636
LPL
3 8 19967385 downstream gene variant T/A;G snv 0.700 1.000 1 2012 2012