Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs328
rs328
LPL
0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 6 2007 2019
dbSNP: rs13702
rs13702
LPL
0.925 0.160 8 19966981 3 prime UTR variant T/A;C snv
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 3 2012 2012
dbSNP: rs13702
rs13702
LPL
0.925 0.160 8 19966981 3 prime UTR variant T/A;C snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 3 2011 2018
dbSNP: rs264
rs264
LPL
0.882 0.080 8 19955669 intron variant G/A snv 0.14
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 3 2009 2013
dbSNP: rs12679834
rs12679834
LPL
8 19962922 intron variant T/C snv 9.4E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 2 2012 2012
dbSNP: rs13702
rs13702
LPL
0.925 0.160 8 19966981 3 prime UTR variant T/A;C snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 2 2011 2018
dbSNP: rs264
rs264
LPL
0.882 0.080 8 19955669 intron variant G/A snv 0.14
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.800 1.000 2 2013 2018
dbSNP: rs264
rs264
LPL
0.882 0.080 8 19955669 intron variant G/A snv 0.14
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 2 2012 2013
dbSNP: rs264
rs264
LPL
0.882 0.080 8 19955669 intron variant G/A snv 0.14
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 2 2012 2013
dbSNP: rs268
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 2 2012 2019
dbSNP: rs268
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 2 2012 2012
dbSNP: rs268
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 2 2012 2019
dbSNP: rs326
rs326
LPL
8 19961928 intron variant A/G snv 0.37
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 2 2008 2019
dbSNP: rs326
rs326
LPL
8 19961928 intron variant A/G snv 0.37
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 2 2012 2013
dbSNP: rs326
rs326
LPL
8 19961928 intron variant A/G snv 0.37
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 2 2012 2019
dbSNP: rs327
rs327
LPL
8 19962025 intron variant T/G snv 0.31
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 2 2012 2012
dbSNP: rs328
rs328
LPL
0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 2 2008 2012
dbSNP: rs328
rs328
LPL
0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 2 2008 2019
dbSNP: rs3289
rs3289
LPL
8 19965681 3 prime UTR variant T/C snv 4.0E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 2 2012 2012
dbSNP: rs3289
rs3289
LPL
8 19965681 3 prime UTR variant T/C snv 4.0E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 2 2012 2012
dbSNP: rs3916027
rs3916027
LPL
8 19967357 downstream gene variant G/A snv 0.31
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 2 2012 2012
dbSNP: rs3916027
rs3916027
LPL
8 19967357 downstream gene variant G/A snv 0.31
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 2 2012 2012
dbSNP: rs3916027
rs3916027
LPL
8 19967357 downstream gene variant G/A snv 0.31
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 2 2012 2012
dbSNP: rs10099160
rs10099160
LPL
8 19964304 intron variant T/G snv 0.20
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs10099160
rs10099160
LPL
8 19964304 intron variant T/G snv 0.20
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012