rs11792480
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11792480(A;A) |
Make rs11792480(A;G) |
Make rs11792480(G;G) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 9 |
Position | 127835846 |
Gene | ENG |
is a | snp |
is | mentioned by |
dbSNP | rs11792480 |
dbSNP (classic) | rs11792480 |
ClinGen | rs11792480 |
ebi | rs11792480 |
HLI | rs11792480 |
Exac | rs11792480 |
Gnomad | rs11792480 |
Varsome | rs11792480 |
LitVar | rs11792480 |
Map | rs11792480 |
PheGenI | rs11792480 |
Biobank | rs11792480 |
1000 genomes | rs11792480 |
hgdp | rs11792480 |
ensembl | rs11792480 |
geneview | rs11792480 |
scholar | rs11792480 |
rs11792480 | |
pharmgkb | rs11792480 |
gwascentral | rs11792480 |
openSNP | rs11792480 |
23andMe | rs11792480 |
SNPshot | rs11792480 |
SNPdbe | rs11792480 |
MSV3d | rs11792480 |
GWAS Ctlg | rs11792480 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 29580923] Endoglin pathway genetic variation in preeclampsia: A validation study in Norwegian and Latina cohorts.
[PMID 29183791] Transforming growth factor beta 1 related gene polymorphisms in gestational hypertension and preeclampsia: A case-control candidate gene association study.