rs17484063
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs17484063(C;C) |
Make rs17484063(C;T) |
Make rs17484063(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 4 |
Position | 148243753 |
Gene | NR3C2 |
is a | snp |
is | mentioned by |
dbSNP | rs17484063 |
dbSNP (classic) | rs17484063 |
ClinGen | rs17484063 |
ebi | rs17484063 |
HLI | rs17484063 |
Exac | rs17484063 |
Gnomad | rs17484063 |
Varsome | rs17484063 |
LitVar | rs17484063 |
Map | rs17484063 |
PheGenI | rs17484063 |
Biobank | rs17484063 |
1000 genomes | rs17484063 |
hgdp | rs17484063 |
ensembl | rs17484063 |
geneview | rs17484063 |
scholar | rs17484063 |
rs17484063 | |
pharmgkb | rs17484063 |
gwascentral | rs17484063 |
openSNP | rs17484063 |
23andMe | rs17484063 |
SNPshot | rs17484063 |
SNPdbe | rs17484063 |
MSV3d | rs17484063 |
GWAS Ctlg | rs17484063 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 26260058] Two novel genetic variants in the mineralocorticoid receptor gene associated with spontaneous preterm birth