rs1531070
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1531070(A;A) |
Make rs1531070(A;G) |
Make rs1531070(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 139874173 |
Gene | MAML3 |
is a | snp |
is | mentioned by |
dbSNP | rs1531070 |
dbSNP (classic) | rs1531070 |
ClinGen | rs1531070 |
ebi | rs1531070 |
HLI | rs1531070 |
Exac | rs1531070 |
Gnomad | rs1531070 |
Varsome | rs1531070 |
LitVar | rs1531070 |
Map | rs1531070 |
PheGenI | rs1531070 |
Biobank | rs1531070 |
1000 genomes | rs1531070 |
hgdp | rs1531070 |
ensembl | rs1531070 |
geneview | rs1531070 |
scholar | rs1531070 |
rs1531070 | |
pharmgkb | rs1531070 |
gwascentral | rs1531070 |
openSNP | rs1531070 |
23andMe | rs1531070 |
SNPshot | rs1531070 |
SNPdbe | rs1531070 |
MSV3d | rs1531070 |
GWAS Ctlg | rs1531070 |
GMAF | 0.2507 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23708190] |
Trait | Congenital heart malformation |
Title | A genome-wide association study identifies two risk loci for congenital heart malformations in Han Chinese populations. |
Risk Allele | A |
P-val | 5E-12 |
Odds Ratio | 1.40 [1.27-1.54] |
[PMID 25875170] Association between the European GWAS-Identified Susceptibility Locus at Chromosome 4p16 and the Risk of Atrial Septal Defect: A Case-Control Study in Southwest China and a Meta-Analysis