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: rs258
rs258
LPL
3 8 19954741 intron variant G/A;C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs271
rs271
LPL
3 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: rs4921683
rs4921683
LPL
3 8 19967557 downstream gene variant T/A snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs13702
rs13702
LPL
3 0.925 0.160 8 19966981 3 prime UTR variant T/A;C snv 0.800 1.000 2 2011 2018
dbSNP: rs320
rs320
LPL
3 0.827 0.200 8 19961566 intron variant T/A;G 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: rs12679834
rs12679834
LPL
5 8 19962922 intron variant T/C snv 9.4E-02 0.700 1.000 2 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: rs255
rs255
LPL
3 8 19954390 intron variant T/C snv 0.17 0.18 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: rs301
rs301
LPL
5 0.925 0.160 8 19959423 intron variant T/C snv 0.24 0.26 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: rs6999612
rs6999612
LPL
3 8 19945573 intron variant T/C snv 7.8E-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: rs327
rs327
LPL
4 8 19962025 intron variant T/G snv 0.31 0.700 1.000 2 2012 2012
dbSNP: rs1800590
rs1800590
LPL
3 8 19939160 intron variant T/G snv 0.13 0.700 1.000 1 2012 2012