rs7246967
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7246967(G;G) |
Make rs7246967(G;T) |
Make rs7246967(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 22873544 |
is a | snp |
is | mentioned by |
dbSNP | rs7246967 |
dbSNP (classic) | rs7246967 |
ClinGen | rs7246967 |
ebi | rs7246967 |
HLI | rs7246967 |
Exac | rs7246967 |
Gnomad | rs7246967 |
Varsome | rs7246967 |
LitVar | rs7246967 |
Map | rs7246967 |
PheGenI | rs7246967 |
Biobank | rs7246967 |
1000 genomes | rs7246967 |
hgdp | rs7246967 |
ensembl | rs7246967 |
geneview | rs7246967 |
scholar | rs7246967 |
rs7246967 | |
pharmgkb | rs7246967 |
gwascentral | rs7246967 |
openSNP | rs7246967 |
23andMe | rs7246967 |
SNPshot | rs7246967 |
SNPdbe | rs7246967 |
MSV3d | rs7246967 |
GWAS Ctlg | rs7246967 |
GMAF | 0.2126 |
Max Magnitude | 0 |
GWAS snp | |
---|---|
PMID | [PMID 23897914] |
Trait | Bronchopulmonary dysplasia |
Title | A genome-wide association study (GWAS) for bronchopulmonary dysplasia. |
Risk Allele | C |
P-val | 4E-6 |
Odds Ratio | 1.40 [NR] |