Have questions? Visit https://www.reddit.com/r/SNPedia

rs7322722

From SNPedia

Orientationplus
Stabilizedplus
Make rs7322722(A;A)
Make rs7322722(A;G)
Make rs7322722(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position77305241
GeneMYCBP2
is asnp
is mentioned by
dbSNPrs7322722
ebirs7322722
HLIrs7322722
Exacrs7322722
Varsomers7322722
Maprs7322722
PheGenIrs7322722
hapmaprs7322722
1000 genomesrs7322722
hgdprs7322722
ensemblrs7322722
gopubmedrs7322722
geneviewrs7322722
scholarrs7322722
googlers7322722
pharmgkbrs7322722
gwascentralrs7322722
openSNPrs7322722
23andMers7322722
23andMe allrs7322722
SNP Nexus

SNPshotrs7322722
SNPdbers7322722
MSV3drs7322722
GWAS Ctlgrs7322722
GMAF0.1791
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 1E-6
Odds Ratio 2.93 [1.90-4.52]