rs2504778
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2504778(A;A) |
Make rs2504778(A;G) |
Make rs2504778(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 27381490 |
Gene | CD164L2 |
is a | snp |
is | mentioned by |
dbSNP | rs2504778 |
dbSNP (classic) | rs2504778 |
ClinGen | rs2504778 |
ebi | rs2504778 |
HLI | rs2504778 |
Exac | rs2504778 |
Gnomad | rs2504778 |
Varsome | rs2504778 |
LitVar | rs2504778 |
Map | rs2504778 |
PheGenI | rs2504778 |
Biobank | rs2504778 |
1000 genomes | rs2504778 |
hgdp | rs2504778 |
ensembl | rs2504778 |
geneview | rs2504778 |
scholar | rs2504778 |
rs2504778 | |
pharmgkb | rs2504778 |
gwascentral | rs2504778 |
openSNP | rs2504778 |
23andMe | rs2504778 |
SNPshot | rs2504778 |
SNPdbe | rs2504778 |
MSV3d | rs2504778 |
GWAS Ctlg | rs2504778 |
GMAF | 0.2792 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 22471352] A Common Genetic Variant of FCN3/CD164L2 Is Associated with Essential Hypertension in a Chinese Population