rs1056819
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1056819(A;A) |
Make rs1056819(A;G) |
Make rs1056819(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 11 |
Position | 2928631 |
Gene | PHLDA2 |
is a | snp |
is | mentioned by |
dbSNP | rs1056819 |
dbSNP (classic) | rs1056819 |
ClinGen | rs1056819 |
ebi | rs1056819 |
HLI | rs1056819 |
Exac | rs1056819 |
Gnomad | rs1056819 |
Varsome | rs1056819 |
LitVar | rs1056819 |
Map | rs1056819 |
PheGenI | rs1056819 |
Biobank | rs1056819 |
1000 genomes | rs1056819 |
hgdp | rs1056819 |
ensembl | rs1056819 |
geneview | rs1056819 |
scholar | rs1056819 |
rs1056819 | |
pharmgkb | rs1056819 |
gwascentral | rs1056819 |
openSNP | rs1056819 |
23andMe | rs1056819 |
SNPshot | rs1056819 |
SNPdbe | rs1056819 |
MSV3d | rs1056819 |
GWAS Ctlg | rs1056819 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 25807806] [Placental PHLDA2 gene imprinting in patients with pre-eclampsia]