rs16835979
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs16835979(A;A) |
Make rs16835979(A;C) |
Make rs16835979(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 4633549 |
Gene | STX18-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs16835979 |
dbSNP (classic) | rs16835979 |
ClinGen | rs16835979 |
ebi | rs16835979 |
HLI | rs16835979 |
Exac | rs16835979 |
Gnomad | rs16835979 |
Varsome | rs16835979 |
LitVar | rs16835979 |
Map | rs16835979 |
PheGenI | rs16835979 |
Biobank | rs16835979 |
1000 genomes | rs16835979 |
hgdp | rs16835979 |
ensembl | rs16835979 |
geneview | rs16835979 |
scholar | rs16835979 |
rs16835979 | |
pharmgkb | rs16835979 |
gwascentral | rs16835979 |
openSNP | rs16835979 |
23andMe | rs16835979 |
SNPshot | rs16835979 |
SNPdbe | rs16835979 |
MSV3d | rs16835979 |
GWAS Ctlg | rs16835979 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 25215500] Replication of the 4p16 Susceptibility Locus in Congenital Heart Disease in Han Chinese Populations
[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