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rs15285

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs15285(A;A)
Make rs15285(A;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position19967156
GeneLPL
is asnp
is mentioned by
dbSNPrs15285
dbSNP (old)rs15285
ClinGenrs15285
ebirs15285
HLIrs15285
Exacrs15285
Gnomadrs15285
Varsomers15285
Maprs15285
PheGenIrs15285
Biobankrs15285
1000 genomesrs15285
hgdprs15285
ensemblrs15285
gopubmedrs15285
geneviewrs15285
scholarrs15285
googlers15285
pharmgkbrs15285
gwascentralrs15285
openSNPrs15285
23andMers15285
23andMe allrs15285
SNPshotrs15285
SNPdbers15285
MSV3drs15285
GWAS Ctlgrs15285
GMAF0.3292
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-10
Odds Ratio 0.2700 [0.19-0.35] unit decrease


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


ClinVar
Risk rs15285(A;A)
Alt rs15285(A;A)
Reference Rs15285(G;G)
Significance Non-pathogenic
Disease Hyperlipoproteinemia
Variation info
Gene LPL
CLNDBN Hyperlipoproteinemia, type I
Reversed 1
HGVS NC_000008.10:g.19824667C>T
CLNSRC
CLNACC RCV000329468.1,