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rs10045497

From SNPedia

Orientationplus
Stabilizedplus
Make rs10045497(A;A)
Make rs10045497(A;C)
Make rs10045497(C;C)
ReferenceGRCh38 38.1/141
Chromosome5
Position75340659
GeneHMGCR
is asnp
is mentioned by
dbSNPrs10045497
dbSNP (classic)rs10045497
ClinGenrs10045497
ebirs10045497
HLIrs10045497
Exacrs10045497
Gnomadrs10045497
Varsomers10045497
LitVarrs10045497
Maprs10045497
PheGenIrs10045497
Biobankrs10045497
1000 genomesrs10045497
hgdprs10045497
ensemblrs10045497
geneviewrs10045497
scholarrs10045497
googlers10045497
pharmgkbrs10045497
gwascentralrs10045497
openSNPrs10045497
23andMers10045497
SNPshotrs10045497
SNPdbers10045497
MSV3drs10045497
GWAS Ctlgrs10045497
Max Magnitude0
? (A;A) (A;C) (C;C) 28


GWAS snp
PMID [PMID 24386095OA-icon.png]
Trait Lipid traits
Title A genome wide association study identifies common variants associated with lipid levels in the Chinese population.
Risk Allele C
P-val 2E-8
Odds Ratio .02 [0.012-0.032] mmol/L increase