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rs11792480

From SNPedia

Orientationplus
Stabilizedplus
Make rs11792480(A;A)
Make rs11792480(A;G)
Make rs11792480(G;G)
ReferenceGRCh38.p7 38.3/151
Chromosome9
Position127835846
GeneENG
is asnp
is mentioned by
dbSNPrs11792480
dbSNP (classic)rs11792480
ClinGenrs11792480
ebirs11792480
HLIrs11792480
Exacrs11792480
Gnomadrs11792480
Varsomers11792480
LitVarrs11792480
Maprs11792480
PheGenIrs11792480
Biobankrs11792480
1000 genomesrs11792480
hgdprs11792480
ensemblrs11792480
geneviewrs11792480
scholarrs11792480
googlers11792480
pharmgkbrs11792480
gwascentralrs11792480
openSNPrs11792480
23andMers11792480
SNPshotrs11792480
SNPdbers11792480
MSV3drs11792480
GWAS Ctlgrs11792480
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 29580923OA-icon.png] 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.