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rs16839962

From SNPedia

Orientationplus
Stabilizedplus
Make rs16839962(A;A)
Make rs16839962(A;T)
Make rs16839962(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position156068774
is asnp
is mentioned by
dbSNPrs16839962
ebirs16839962
HLIrs16839962
Exacrs16839962
Varsomers16839962
Maprs16839962
PheGenIrs16839962
hapmaprs16839962
1000 genomesrs16839962
hgdprs16839962
ensemblrs16839962
gopubmedrs16839962
geneviewrs16839962
scholarrs16839962
googlers16839962
pharmgkbrs16839962
gwascentralrs16839962
openSNPrs16839962
23andMers16839962
23andMe allrs16839962
SNP Nexus

SNPshotrs16839962
SNPdbers16839962
MSV3drs16839962
GWAS Ctlgrs16839962
GMAF0.2369
Max Magnitude
? (A;A) (A;T) (T;T) 28
GWAS snp
PMID [PMID 20339536OA-icon.png]
Trait Response to statin therapy
Title Genome-wide association of lipid-lowering response to statins in combined study populations
Risk Allele T
P-val 0.000009
Odds Ratio None None