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rs11668477

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0
Make rs11668477(A;G)
Make rs11668477(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position11084354
is asnp
is mentioned by
dbSNPrs11668477
ebirs11668477
HLIrs11668477
Exacrs11668477
Varsomers11668477
Maprs11668477
PheGenIrs11668477
hapmaprs11668477
1000 genomesrs11668477
hgdprs11668477
ensemblrs11668477
gopubmedrs11668477
geneviewrs11668477
scholarrs11668477
googlers11668477
pharmgkbrs11668477
gwascentralrs11668477
openSNPrs11668477
23andMers11668477
23andMe allrs11668477
SNP Nexus

SNPshotrs11668477
SNPdbers11668477
MSV3drs11668477
GWAS Ctlgrs11668477
GMAF0.2966
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19060910OA-icon.png]
Trait LDL cholesterol
Title Genome-wide association analysis of metabolic traits in a birth cohort from a founder population
Risk Allele G
P-val 2E-7
Odds Ratio 0.13 [0.08-0.17] mmol/l decrease



[PMID 17239995] Genetic study evaluating LDLR polymorphisms and Alzheimer's disease.


[PMID 18262040OA-icon.png] LDL-cholesterol concentrations: a genome-wide association study.


GET Evidence
rs11668477
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.401639
summary