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rs11649653

From SNPedia

Orientationplus
Stabilizedplus
Make rs11649653(C;C)
Make rs11649653(C;G)
Make rs11649653(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position30907166
GeneLOC100289419
is asnp
is mentioned by
dbSNPrs11649653
dbSNP (classic)rs11649653
ClinGenrs11649653
ebirs11649653
HLIrs11649653
Exacrs11649653
Gnomadrs11649653
Varsomers11649653
LitVarrs11649653
Maprs11649653
PheGenIrs11649653
Biobankrs11649653
1000 genomesrs11649653
hgdprs11649653
ensemblrs11649653
geneviewrs11649653
scholarrs11649653
googlers11649653
pharmgkbrs11649653
gwascentralrs11649653
openSNPrs11649653
23andMers11649653
SNPshotrs11649653
SNPdbers11649653
MSV3drs11649653
GWAS Ctlgrs11649653
GMAF0.4591
Max Magnitude0
? (C;C) (C;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 G
P-val 3E-8
Odds Ratio 2.1300 None
GWAS snp
PMID [PMID 24097068OA-icon.png]
Trait Triglycerides
Title Discovery and refinement of loci associated with lipid levels.
Risk Allele G
P-val 2E-7
Odds Ratio .03 [NR] mg/dL decrease