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rs10121110

From SNPedia

Orientationplus
Stabilizedplus
Make rs10121110(A;A)
Make rs10121110(A;G)
Make rs10121110(G;G)
ReferenceGRCh38.p7 38.3/151
Chromosome9
Position127840129
GeneENG
is asnp
is mentioned by
dbSNPrs10121110
dbSNP (classic)rs10121110
ClinGenrs10121110
ebirs10121110
HLIrs10121110
Exacrs10121110
Gnomadrs10121110
Varsomers10121110
LitVarrs10121110
Maprs10121110
PheGenIrs10121110
Biobankrs10121110
1000 genomesrs10121110
hgdprs10121110
ensemblrs10121110
geneviewrs10121110
scholarrs10121110
googlers10121110
pharmgkbrs10121110
gwascentralrs10121110
openSNPrs10121110
23andMers10121110
23andMe allrs10121110
SNPshotrs10121110
SNPdbers10121110
MSV3drs10121110
GWAS Ctlgrs10121110
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.