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rs729397

From SNPedia

Orientationminus
Stabilizedminus
Make rs729397(C;C)
Make rs729397(C;G)
Make rs729397(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position2489827
is asnp
is mentioned by
dbSNPrs729397
ebirs729397
HLIrs729397
Exacrs729397
Varsomers729397
Maprs729397
PheGenIrs729397
hapmaprs729397
1000 genomesrs729397
hgdprs729397
ensemblrs729397
gopubmedrs729397
geneviewrs729397
scholarrs729397
googlers729397
pharmgkbrs729397
gwascentralrs729397
openSNPrs729397
23andMers729397
23andMe allrs729397
SNP Nexus

SNPshotrs729397
SNPdbers729397
MSV3drs729397
GWAS Ctlgrs729397
GMAF0.2245
Max Magnitude
? (C;C) (C;G) (G;G) 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 C
P-val 0.000008
Odds Ratio None None

[PMID 16400611OA-icon.png] Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample.