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rs9976946

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0
Make rs9976946(C;C)
Make rs9976946(C;T)
ReferenceGRCh38 38.1/141
Chromosome21
Position34835765
GeneRUNX1
is asnp
is mentioned by
dbSNPrs9976946
ebirs9976946
HLIrs9976946
Exacrs9976946
Varsomers9976946
Maprs9976946
PheGenIrs9976946
hapmaprs9976946
1000 genomesrs9976946
hgdprs9976946
ensemblrs9976946
gopubmedrs9976946
geneviewrs9976946
scholarrs9976946
googlers9976946
pharmgkbrs9976946
gwascentralrs9976946
openSNPrs9976946
23andMers9976946
23andMe allrs9976946
SNP Nexus

SNPshotrs9976946
SNPdbers9976946
MSV3drs9976946
GWAS Ctlgrs9976946
GMAF0.007346
Max Magnitude0
? (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 5E-6
Odds Ratio 5.50 [2.65-11.39]