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rs12641856

From SNPedia

Orientationplus
Stabilizedplus
Make rs12641856(A;A)
Make rs12641856(A;G)
Make rs12641856(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position181688712
is asnp
is mentioned by
dbSNPrs12641856
ebirs12641856
HLIrs12641856
Exacrs12641856
Varsomers12641856
Maprs12641856
PheGenIrs12641856
hapmaprs12641856
1000 genomesrs12641856
hgdprs12641856
ensemblrs12641856
gopubmedrs12641856
geneviewrs12641856
scholarrs12641856
googlers12641856
pharmgkbrs12641856
gwascentralrs12641856
openSNPrs12641856
23andMers12641856
23andMe allrs12641856
SNP Nexus

SNPshotrs12641856
SNPdbers12641856
MSV3drs12641856
GWAS Ctlgrs12641856
GMAF0.05739
Max Magnitude
? (A;A) (A;G) (G;G) 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 15.19 [4.98-46.35]