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rs1531070

From SNPedia

Orientationplus
Stabilizedplus
Make rs1531070(A;A)
Make rs1531070(A;G)
Make rs1531070(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position139874173
GeneMAML3
is asnp
is mentioned by
dbSNPrs1531070
ebirs1531070
HLIrs1531070
Exacrs1531070
Varsomers1531070
Maprs1531070
PheGenIrs1531070
hapmaprs1531070
1000 genomesrs1531070
hgdprs1531070
ensemblrs1531070
gopubmedrs1531070
geneviewrs1531070
scholarrs1531070
googlers1531070
pharmgkbrs1531070
gwascentralrs1531070
openSNPrs1531070
23andMers1531070
23andMe allrs1531070
SNP Nexus

SNPshotrs1531070
SNPdbers1531070
MSV3drs1531070
GWAS Ctlgrs1531070
GMAF0.2507
Max Magnitude
? (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 25875170OA-icon.png] 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