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rs13702

From SNPedia

Orientationminus
Stabilizedminus
Make rs13702(A;A)
Make rs13702(A;G)
Make rs13702(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position19966981
GeneLPL
is asnp
is mentioned by
dbSNPrs13702
dbSNP (classic)rs13702
ClinGenrs13702
ebirs13702
HLIrs13702
Exacrs13702
Gnomadrs13702
Varsomers13702
LitVarrs13702
Maprs13702
PheGenIrs13702
Biobankrs13702
1000 genomesrs13702
hgdprs13702
ensemblrs13702
geneviewrs13702
scholarrs13702
googlers13702
pharmgkbrs13702
gwascentralrs13702
openSNPrs13702
23andMers13702
SNPshotrs13702
SNPdbers13702
MSV3drs13702
GWAS Ctlgrs13702
GMAF0.332
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 21386085OA-icon.png]
Trait
Title A Bivariate Genome-Wide Approach to Metabolic Syndrome: STAMPEED Consortium
Risk Allele A
P-val 1E-16
Odds Ratio 0.2900 [0.23-0.35] unit increase


[PMID 19041386OA-icon.png] Genetic-epidemiological evidence on genes associated with HDL cholesterol levels: a systematic in-depth review.


[PMID 25814643OA-icon.png] Genetic Variations in MicroRNA-Binding Sites Affect MicroRNA-Mediated Regulation of Several Genes Associated With Cardio-metabolic Phenotypes.


[PMID 19148283OA-icon.png] Genetic differences between the determinants of lipid profile phenotypes in African and European Americans: the Jackson Heart Study.


[PMID 19299407OA-icon.png] Replication of genetic associations with plasma lipoprotein traits in a multiethnic sample.


[PMID 20150529OA-icon.png] Associations of lipoprotein lipase gene polymorphisms with longitudinal plasma lipid trends in young adults: The Coronary Artery Risk Development in Young Adults (CARDIA) study.


[PMID 20416077OA-icon.png] Identification of type 2 diabetes-associated combination of SNPs using support vector machine.


[PMID 25156894OA-icon.png] Lipoprotein lipase variants interact with polyunsaturated fatty acids for obesity traits in women: Replication in two populations


ClinVar
Risk rs13702(G;G)
Alt rs13702(G;G)
Reference rs13702(A;A)
Significance Other
Disease High density lipoprotein cholesterol level quantitative trait locus 11 Hyperlipoproteinemia
Variation info
Gene LPL
CLNDBN High density lipoprotein cholesterol level quantitative trait locus 11 Hyperlipoproteinemia, type I
Reversed 1
HGVS NC_000008.10:g.19824492T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000033176.2, RCV000353989.1,