rs10989019
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10989019(C;C) |
Make rs10989019(C;T) |
Make rs10989019(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 100214259 |
Gene | INVS |
is a | snp |
is | mentioned by |
dbSNP | rs10989019 |
dbSNP (classic) | rs10989019 |
ClinGen | rs10989019 |
ebi | rs10989019 |
HLI | rs10989019 |
Exac | rs10989019 |
Gnomad | rs10989019 |
Varsome | rs10989019 |
LitVar | rs10989019 |
Map | rs10989019 |
PheGenI | rs10989019 |
Biobank | rs10989019 |
1000 genomes | rs10989019 |
hgdp | rs10989019 |
ensembl | rs10989019 |
geneview | rs10989019 |
scholar | rs10989019 |
rs10989019 | |
pharmgkb | rs10989019 |
gwascentral | rs10989019 |
openSNP | rs10989019 |
23andMe | rs10989019 |
SNPshot | rs10989019 |
SNPdbe | rs10989019 |
MSV3d | rs10989019 |
GWAS Ctlg | rs10989019 |
GMAF | 0.1612 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 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 | 2E-6 |
Odds Ratio | 3.21 [1.98-5.20] |