Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4420638
rs4420638
APOC1
G 0.700 GeneticVariation GWASDB Biological, clinical and population relevance of 95 loci for blood lipids. 20686565

2010
dbSNP: rs514230
rs514230
LINC01132
A 0.700 GeneticVariation GWASDB Biological, clinical and population relevance of 95 loci for blood lipids. 20686565

2010
dbSNP: rs6029526
rs6029526
TOP1
T 0.700 GeneticVariation GWASDB Biological, clinical and population relevance of 95 loci for blood lipids. 20686565

2010
dbSNP: rs629301
rs629301
CELSR2
G 0.700 GeneticVariation GWASDB Biological, clinical and population relevance of 95 loci for blood lipids. 20686565

2010
dbSNP: rs635634
rs635634 		T 0.700 GeneticVariation GWASDB Biological, clinical and population relevance of 95 loci for blood lipids. 20686565

2010
dbSNP: rs6511720
rs6511720
LDLR
T 0.700 GeneticVariation GWASDB Biological, clinical and population relevance of 95 loci for blood lipids. 20686565

2010
dbSNP: rs6882076
rs6882076
TIMD4
T 0.700 GeneticVariation GWASDB Biological, clinical and population relevance of 95 loci for blood lipids. 20686565

2010
dbSNP: rs7206971
rs7206971
EFCAB13
T 0.700 GeneticVariation GWASDB Biological, clinical and population relevance of 95 loci for blood lipids. 20686565

2010
dbSNP: rs8017377
rs8017377
NYNRIN
T 0.700 GeneticVariation GWASDB Biological, clinical and population relevance of 95 loci for blood lipids. 20686565

2010
dbSNP: rs9488822
rs9488822
FRK
T 0.700 GeneticVariation GWASDB Biological, clinical and population relevance of 95 loci for blood lipids. 20686565

2010
dbSNP: rs964184
rs964184
ZPR1
G 0.700 GeneticVariation GWASDB Biological, clinical and population relevance of 95 loci for blood lipids. 20686565

2010
dbSNP: rs9987289
rs9987289
LOC157273
T 0.700 GeneticVariation GWASDB Biological, clinical and population relevance of 95 loci for blood lipids. 20686565

2010
dbSNP: rs11591147
rs11591147
PCSK9
0.700 GeneticVariation GWASDB Common and low-frequency genetic variants in the PCSK9 locus influence circulating PCSK9 levels. 22460556

2012
dbSNP: rs4420638
rs4420638
APOC1
0.700 GeneticVariation GWASDB Common SNPs in HMGCR in micronesians and whites associated with LDL-cholesterol levels affect alternative splicing of exon13. 18802019

2008
dbSNP: rs7703051
rs7703051 		A 0.700 GeneticVariation GWASDB Common SNPs in HMGCR in micronesians and whites associated with LDL-cholesterol levels affect alternative splicing of exon13. 18802019

2008
dbSNP: rs10401969
rs10401969
SUGP1
C 0.700 GeneticVariation GWASDB Common variants at 30 loci contribute to polygenic dyslipidemia. 19060906

2009
dbSNP: rs11206510
rs11206510 		C 0.700 GeneticVariation GWASDB Common variants at 30 loci contribute to polygenic dyslipidemia. 19060906

2009
dbSNP: rs12740374
rs12740374
CELSR2
T 0.700 GeneticVariation GWASDB Common variants at 30 loci contribute to polygenic dyslipidemia. 19060906

2009
dbSNP: rs1501908
rs1501908 		G 0.700 GeneticVariation GWASDB Common variants at 30 loci contribute to polygenic dyslipidemia. 19060906

2009
dbSNP: rs2650000
rs2650000
HNF1A-AS1
A 0.700 GeneticVariation GWASDB Common variants at 30 loci contribute to polygenic dyslipidemia. 19060906

2009
dbSNP: rs3846663
rs3846663
HMGCR ; CERT1
T 0.700 GeneticVariation GWASDB Common variants at 30 loci contribute to polygenic dyslipidemia. 19060906

2009
dbSNP: rs4420638
rs4420638
APOC1
G 0.700 GeneticVariation GWASDB Common variants at 30 loci contribute to polygenic dyslipidemia. 19060906

2009
dbSNP: rs515135
rs515135 		T 0.700 GeneticVariation GWASDB Common variants at 30 loci contribute to polygenic dyslipidemia. 19060906

2009
dbSNP: rs6102059
rs6102059
LOC102724968
T 0.700 GeneticVariation GWASDB Common variants at 30 loci contribute to polygenic dyslipidemia. 19060906

2009
dbSNP: rs6511720
rs6511720
LDLR
T 0.700 GeneticVariation GWASDB Common variants at 30 loci contribute to polygenic dyslipidemia. 19060906

2009