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rs11776767

From SNPedia

Orientationplus
Stabilizedplus
Make rs11776767(C;C)
Make rs11776767(C;G)
Make rs11776767(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position10826419
GenePINX1
is asnp
is mentioned by
dbSNPrs11776767
ebirs11776767
HLIrs11776767
Exacrs11776767
Varsomers11776767
Maprs11776767
PheGenIrs11776767
hapmaprs11776767
1000 genomesrs11776767
hgdprs11776767
ensemblrs11776767
gopubmedrs11776767
geneviewrs11776767
scholarrs11776767
googlers11776767
pharmgkbrs11776767
gwascentralrs11776767
openSNPrs11776767
23andMers11776767
23andMe allrs11776767
SNP Nexus

SNPshotrs11776767
SNPdbers11776767
MSV3drs11776767
GWAS Ctlgrs11776767
GMAF0.4215
Max Magnitude
? (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 C
P-val 1E-8
Odds Ratio 2.0100 None
GWAS snp
PMID [PMID 24097068OA-icon.png]
Trait Triglycerides
Title Discovery and refinement of loci associated with lipid levels.
Risk Allele C
P-val 3E-11
Odds Ratio .02 [NR] mg/dL increase