rs10121110
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10121110(A;A) |
Make rs10121110(A;G) |
Make rs10121110(G;G) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 9 |
Position | 127840129 |
Gene | ENG |
is a | snp |
is | mentioned by |
dbSNP | rs10121110 |
dbSNP (classic) | rs10121110 |
ClinGen | rs10121110 |
ebi | rs10121110 |
HLI | rs10121110 |
Exac | rs10121110 |
Gnomad | rs10121110 |
Varsome | rs10121110 |
LitVar | rs10121110 |
Map | rs10121110 |
PheGenI | rs10121110 |
Biobank | rs10121110 |
1000 genomes | rs10121110 |
hgdp | rs10121110 |
ensembl | rs10121110 |
geneview | rs10121110 |
scholar | rs10121110 |
rs10121110 | |
pharmgkb | rs10121110 |
gwascentral | rs10121110 |
openSNP | rs10121110 |
23andMe | rs10121110 |
SNPshot | rs10121110 |
SNPdbe | rs10121110 |
MSV3d | rs10121110 |
GWAS Ctlg | rs10121110 |
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.