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rs7671266

From SNPedia

Orientationplus
Stabilizedplus
Make rs7671266(C;C)
Make rs7671266(C;T)
Make rs7671266(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position10054752
is asnp
is mentioned by
dbSNPrs7671266
ebirs7671266
HLIrs7671266
Exacrs7671266
Varsomers7671266
Maprs7671266
PheGenIrs7671266
hapmaprs7671266
1000 genomesrs7671266
hgdprs7671266
ensemblrs7671266
gopubmedrs7671266
geneviewrs7671266
scholarrs7671266
googlers7671266
pharmgkbrs7671266
gwascentralrs7671266
openSNPrs7671266
23andMers7671266
23andMe allrs7671266
SNP Nexus

SNPshotrs7671266
SNPdbers7671266
MSV3drs7671266
GWAS Ctlgrs7671266
GMAF0.2153
Max Magnitude
? (C;C) (C;T) (T;T) 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 9E-71
Odds Ratio 0.3050 [0.27-0.34] umol/l decrease