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rs2240466

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common on affy axiom data
Make rs2240466(C;T)
Make rs2240466(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position73441939
GeneBAZ1B
is asnp
is mentioned by
dbSNPrs2240466
ebirs2240466
HLIrs2240466
Exacrs2240466
Varsomers2240466
Maprs2240466
PheGenIrs2240466
hapmaprs2240466
1000 genomesrs2240466
hgdprs2240466
ensemblrs2240466
gopubmedrs2240466
geneviewrs2240466
scholarrs2240466
googlers2240466
pharmgkbrs2240466
gwascentralrs2240466
openSNPrs2240466
23andMers2240466
23andMe allrs2240466
SNP Nexus

SNPshotrs2240466
SNPdbers2240466
MSV3drs2240466
GWAS Ctlgrs2240466
GMAF0.0877
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19060911OA-icon.png]
Trait Triglycerides
Title Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts
Risk Allele G
P-val 1E-12
Odds Ratio 0.14 [NR] SD increase


GWAS snp
PMID [PMID 21490707OA-icon.png]
Trait
Title Genome-wide meta-analysis identifies regions on 7p21 (AHR) and 15q24 (CYP1A2) as determinants of habitual caffeine consumption.
Risk Allele A
P-val 0.000001
Odds Ratio 0.1109 [0.07-0.15] mg/day increase

[PMID 19185284OA-icon.png] Common variation in the beta-carotene 15,15'-monooxygenase 1 gene affects circulating levels of carotenoids: a genome-wide association study.

[PMID 19435741OA-icon.png] Common lipid-altering gene variants are associated with therapeutic intervention thresholds of lipid levels in older people.

[PMID 20502693OA-icon.png] Genetics and beyond--the transcriptome of human monocytes and disease susceptibility.


GET Evidence
rs2240466
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.101562
summary



[PMID 26252223OA-icon.png] Genetic Variants Associated with Lipid Profiles in Chinese Patients with Type 2 Diabetes