rs11617740
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11617740(A;A) |
Make rs11617740(A;G) |
Make rs11617740(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 102027776 |
Gene | FGF14 |
is a | snp |
is | mentioned by |
dbSNP | rs11617740 |
dbSNP (classic) | rs11617740 |
ClinGen | rs11617740 |
ebi | rs11617740 |
HLI | rs11617740 |
Exac | rs11617740 |
Gnomad | rs11617740 |
Varsome | rs11617740 |
LitVar | rs11617740 |
Map | rs11617740 |
PheGenI | rs11617740 |
Biobank | rs11617740 |
1000 genomes | rs11617740 |
hgdp | rs11617740 |
ensembl | rs11617740 |
geneview | rs11617740 |
scholar | rs11617740 |
rs11617740 | |
pharmgkb | rs11617740 |
gwascentral | rs11617740 |
openSNP | rs11617740 |
23andMe | rs11617740 |
SNPshot | rs11617740 |
SNPdbe | rs11617740 |
MSV3d | rs11617740 |
GWAS Ctlg | rs11617740 |
GMAF | 0.03673 |
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 | 7E-7 |
Odds Ratio | 16.69 [5.53-51.97] |