rs714052
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common on affy axiom data |
Make rs714052(C;C) |
Make rs714052(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 73450539 |
Gene | BAZ1B |
is a | snp |
is | mentioned by |
dbSNP | rs714052 |
dbSNP (classic) | rs714052 |
ClinGen | rs714052 |
ebi | rs714052 |
HLI | rs714052 |
Exac | rs714052 |
Gnomad | rs714052 |
Varsome | rs714052 |
LitVar | rs714052 |
Map | rs714052 |
PheGenI | rs714052 |
Biobank | rs714052 |
1000 genomes | rs714052 |
hgdp | rs714052 |
ensembl | rs714052 |
geneview | rs714052 |
scholar | rs714052 |
rs714052 | |
pharmgkb | rs714052 |
gwascentral | rs714052 |
openSNP | rs714052 |
23andMe | rs714052 |
SNPshot | rs714052 |
SNPdbe | rs714052 |
MSV3d | rs714052 |
GWAS Ctlg | rs714052 |
GMAF | 0.08815 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 19060906] |
Trait | Triglycerides |
Title | Common variants at 30 loci contribute to polygenic dyslipidemia |
Risk Allele | G |
P-val | 3E-15 |
Odds Ratio | 0.16 [0.10-0.22] SD decrease |
GWAS snp | |
---|---|
PMID | [PMID 20657596] |
Trait | Hypertriglyceridemia |
Title | Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia |
Risk Allele | |
P-val | 0.000003 |
Odds Ratio | 2.27 [1.61-3.23] |
GWAS snp | |
---|---|
PMID | [PMID 20139978] |
Trait | Triglycerides |
Title | Genome-wide association study of hematological and biochemical traits in a Japanese population. |
Risk Allele | G |
P-val | 3E-7 |
Odds Ratio | .12 [0.076-0.170] unit decrease |