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rs10989019

From SNPedia

Orientationplus
Stabilizedplus
Make rs10989019(C;C)
Make rs10989019(C;T)
Make rs10989019(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position100214259
GeneINVS
is asnp
is mentioned by
dbSNPrs10989019
ebirs10989019
HLIrs10989019
Exacrs10989019
Varsomers10989019
Maprs10989019
PheGenIrs10989019
hapmaprs10989019
1000 genomesrs10989019
hgdprs10989019
ensemblrs10989019
gopubmedrs10989019
geneviewrs10989019
scholarrs10989019
googlers10989019
pharmgkbrs10989019
gwascentralrs10989019
openSNPrs10989019
23andMers10989019
23andMe allrs10989019
SNP Nexus

SNPshotrs10989019
SNPdbers10989019
MSV3drs10989019
GWAS Ctlgrs10989019
GMAF0.1612
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23551011OA-icon.png]
Trait Preeclampsia
Title Genome-Wide Association Study of Pre-Eclampsia Detects Novel Maternal Single Nucleotide Polymorphisms and Copy-Number Variants in Subsets of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) Study Cohort.
Risk Allele
P-val 2E-6
Odds Ratio 3.21 [1.98-5.20]