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rs2266788

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common on affy axiom data
Make rs2266788(C;C)
Make rs2266788(C;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position116789970
GeneAPOA5, ZNF259
is asnp
is mentioned by
dbSNPrs2266788
ebirs2266788
HLIrs2266788
Exacrs2266788
Varsomers2266788
Maprs2266788
PheGenIrs2266788
hapmaprs2266788
1000 genomesrs2266788
hgdprs2266788
ensemblrs2266788
gopubmedrs2266788
geneviewrs2266788
scholarrs2266788
googlers2266788
pharmgkbrs2266788
gwascentralrs2266788
openSNPrs2266788
23andMers2266788
23andMe allrs2266788
SNP Nexus

SNPshotrs2266788
SNPdbers2266788
MSV3drs2266788
GWAS Ctlgrs2266788
GMAF0.1134
Max Magnitude0
? (C;C) (C;T) (T;T) 28

[PMID 19732897] Associations of polymorphisms in the apolipoprotein A1/C3/A4/A5 gene cluster with familial combined hyperlipidaemia in Hong Kong Chinese


[PMID 20395964] Different effects of apolipoprotein A5 SNPs and haplotypes on triglyceride concentration in three ethnic origins

[PMID 20883102] Haplotype analysis of the apolipoprotein A5 gene in obese pediatric patients

GWAS snp
PMID [PMID 21386085OA-icon.png]
Trait
Title A Bivariate Genome-Wide Approach to Metabolic Syndrome: STAMPEED Consortium
Risk Allele A
P-val 2E-16
Odds Ratio 0.4100 [0.31-0.51] unit increase


[PMID 21375366] Impact of apolipoprotein A5 (APOA5) polymorphisms on serum triglyceride levels in schizophrenic patients under long-term atypical antipsychotic treatment


[PMID 19041386OA-icon.png] Genetic-epidemiological evidence on genes associated with HDL cholesterol levels: a systematic in-depth review.


[PMID 19197348OA-icon.png] Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae.


[PMID 20452521OA-icon.png] Triglyceride-mediated pathways and coronary disease: collaborative analysis of 101 studies.


ClinVar
Risk rs2266788(T;T)
Alt rs2266788(T;T)
Reference rs2266788(C;C)
Significance Other
Disease Hypertriglyceridemia
Variation info
Gene ZPR1 APOA5
CLNDBN Hypertriglyceridemia, susceptibility to
Reversed 1
HGVS NC_000011.9:g.116660686G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000114996.2,