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rs10782529

From SNPedia

Orientationplus
Stabilizedplus
Make rs10782529(C;C)
Make rs10782529(C;T)
Make rs10782529(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position84802560
is asnp
is mentioned by
dbSNPrs10782529
dbSNP (classic)rs10782529
ClinGenrs10782529
ebirs10782529
HLIrs10782529
Exacrs10782529
Gnomadrs10782529
Varsomers10782529
LitVarrs10782529
Maprs10782529
PheGenIrs10782529
Biobankrs10782529
1000 genomesrs10782529
hgdprs10782529
ensemblrs10782529
geneviewrs10782529
scholarrs10782529
googlers10782529
pharmgkbrs10782529
gwascentralrs10782529
openSNPrs10782529
23andMers10782529
SNPshotrs10782529
SNPdbers10782529
MSV3drs10782529
GWAS Ctlgrs10782529
GMAF0.348
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 23118302]
Trait Lipoprotein-associated phospholipase A2 activity change in response to statin therapy
Title Genome-wide association study evaluating lipoprotein-associated phospholipase A2 mass and activity at baseline and after rosuvastatin therapy.
Risk Allele C
P-val 4E-6
Odds Ratio 1.70 [1.11-2.29] percent increase