rs7322722
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7322722(A;A) |
Make rs7322722(A;G) |
Make rs7322722(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 77305241 |
Gene | MYCBP2 |
is a | snp |
is | mentioned by |
dbSNP | rs7322722 |
dbSNP (classic) | rs7322722 |
ClinGen | rs7322722 |
ebi | rs7322722 |
HLI | rs7322722 |
Exac | rs7322722 |
Gnomad | rs7322722 |
Varsome | rs7322722 |
LitVar | rs7322722 |
Map | rs7322722 |
PheGenI | rs7322722 |
Biobank | rs7322722 |
1000 genomes | rs7322722 |
hgdp | rs7322722 |
ensembl | rs7322722 |
geneview | rs7322722 |
scholar | rs7322722 |
rs7322722 | |
pharmgkb | rs7322722 |
gwascentral | rs7322722 |
openSNP | rs7322722 |
23andMe | rs7322722 |
SNPshot | rs7322722 |
SNPdbe | rs7322722 |
MSV3d | rs7322722 |
GWAS Ctlg | rs7322722 |
GMAF | 0.1791 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23551011] |
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] |