rs2240466

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common on affy axiom data

Make rs2240466(C;T)

Make rs2240466(T;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

73441939

Gene

BAZ1B

is a	snp
is	mentioned by
dbSNP	rs2240466
dbSNP (classic)	rs2240466
ClinGen	rs2240466
ebi	rs2240466
HLI	rs2240466
Exac	rs2240466
Gnomad	rs2240466
Varsome	rs2240466
LitVar	rs2240466
Map	rs2240466
PheGenI	rs2240466
Biobank	rs2240466
1000 genomes	rs2240466
hgdp	rs2240466
ensembl	rs2240466
geneview	rs2240466
scholar	rs2240466
google	rs2240466
pharmgkb	rs2240466
gwascentral	rs2240466
openSNP	rs2240466
23andMe	rs2240466
SNPshot	rs2240466
SNPdbe	rs2240466
MSV3d	rs2240466
GWAS Ctlg	rs2240466

GMAF

0.0877

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

GWAS snp
PMID	[PMID 19060911]
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 21490707]
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 19185284] Common variation in the beta-carotene 15,15'-monooxygenase 1 gene affects circulating levels of carotenoids: a genome-wide association study.

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

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

[PMID 26252223] Genetic Variants Associated with Lipid Profiles in Chinese Patients with Type 2 Diabetes