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rs9733352

From SNPedia

Orientationplus
Stabilizedplus
Make rs9733352(C;C)
Make rs9733352(C;G)
Make rs9733352(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position126979126
GeneDOCK1
is asnp
is mentioned by
dbSNPrs9733352
ebirs9733352
HLIrs9733352
Exacrs9733352
Varsomers9733352
Maprs9733352
PheGenIrs9733352
hapmaprs9733352
1000 genomesrs9733352
hgdprs9733352
ensemblrs9733352
gopubmedrs9733352
geneviewrs9733352
scholarrs9733352
googlers9733352
pharmgkbrs9733352
gwascentralrs9733352
openSNPrs9733352
23andMers9733352
23andMe allrs9733352
SNP Nexus

SNPshotrs9733352
SNPdbers9733352
MSV3drs9733352
GWAS Ctlgrs9733352
GMAF0.4706
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 23031429OA-icon.png]
Trait Apolipoprotein Levels
Title A Genome-Wide Association Study of Monozygotic Twin-Pairs Suggests a Locus Related to Variability of Serum High-Density Lipoprotein Cholesterol.
Risk Allele C
P-val 4E-8
Odds Ratio .06 [0.038-0.082] unit increase