rs730532
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs730532(C;C) |
Make rs730532(C;T) |
Make rs730532(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 14 |
Position | 52052093 |
Gene | NID2 |
is a | snp |
is | mentioned by |
dbSNP | rs730532 |
dbSNP (classic) | rs730532 |
ClinGen | rs730532 |
ebi | rs730532 |
HLI | rs730532 |
Exac | rs730532 |
Gnomad | rs730532 |
Varsome | rs730532 |
LitVar | rs730532 |
Map | rs730532 |
PheGenI | rs730532 |
Biobank | rs730532 |
1000 genomes | rs730532 |
hgdp | rs730532 |
ensembl | rs730532 |
geneview | rs730532 |
scholar | rs730532 |
rs730532 | |
pharmgkb | rs730532 |
gwascentral | rs730532 |
openSNP | rs730532 |
23andMe | rs730532 |
SNPshot | rs730532 |
SNPdbe | rs730532 |
MSV3d | rs730532 |
GWAS Ctlg | rs730532 |
GMAF | 0.3898 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 17903307] |
Trait | Other pulmonary function traits |
Title | Framingham Heart Study genome-wide association: results for pulmonary function measures |
Risk Allele | |
P-val | 0.0000060000000000000002 |
Odds Ratio | NR NR |
[PMID 17903299] A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study.