Have questions? Visit https://www.reddit.com/r/SNPedia

rs508487

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs508487(A;A)
Make rs508487(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position117204850
GenePCSK7, TAGLN
is asnp
is mentioned by
dbSNPrs508487
ebirs508487
HLIrs508487
Exacrs508487
Varsomers508487
Maprs508487
PheGenIrs508487
hapmaprs508487
1000 genomesrs508487
hgdprs508487
ensemblrs508487
gopubmedrs508487
geneviewrs508487
scholarrs508487
googlers508487
pharmgkbrs508487
gwascentralrs508487
openSNPrs508487
23andMers508487
23andMe allrs508487
SNP Nexus

SNPshotrs508487
SNPdbers508487
MSV3drs508487
GWAS Ctlgrs508487
GMAF0.07484
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21943158OA-icon.png]
Trait
Title Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits.
Risk Allele T
P-val 2E-10
Odds Ratio 0.2350 [0.16-0.31] mmol/l increase