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rs635634

From SNPedia

Orientationminus
Stabilizedminus
Make rs635634(A;A)
Make rs635634(A;G)
Make rs635634(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position133279427
is asnp
is mentioned by
dbSNPrs635634
dbSNP (classic)rs635634
ClinGenrs635634
ebirs635634
HLIrs635634
Exacrs635634
Gnomadrs635634
Varsomers635634
LitVarrs635634
Maprs635634
PheGenIrs635634
Biobankrs635634
1000 genomesrs635634
hgdprs635634
ensemblrs635634
geneviewrs635634
scholarrs635634
googlers635634
pharmgkbrs635634
gwascentralrs635634
openSNPrs635634
23andMers635634
SNPshotrs635634
SNPdbers635634
MSV3drs635634
GWAS Ctlgrs635634
Merged fromRs9411489
GMAF0.1644
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 20686565OA-icon.png]
Trait
Title Biological, clinical and population relevance of 95 loci for blood lipids.
Risk Allele T
P-val 8E-22
Odds Ratio 2.0500 None