rs7326277
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7326277(C;C) |
Make rs7326277(C;T) |
Make rs7326277(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 28302077 |
Gene | FLT1 |
is a | snp |
is | mentioned by |
dbSNP | rs7326277 |
dbSNP (classic) | rs7326277 |
ClinGen | rs7326277 |
ebi | rs7326277 |
HLI | rs7326277 |
Exac | rs7326277 |
Gnomad | rs7326277 |
Varsome | rs7326277 |
LitVar | rs7326277 |
Map | rs7326277 |
PheGenI | rs7326277 |
Biobank | rs7326277 |
1000 genomes | rs7326277 |
hgdp | rs7326277 |
ensembl | rs7326277 |
geneview | rs7326277 |
scholar | rs7326277 |
rs7326277 | |
pharmgkb | rs7326277 |
gwascentral | rs7326277 |
openSNP | rs7326277 |
23andMe | rs7326277 |
SNPshot | rs7326277 |
SNPdbe | rs7326277 |
MSV3d | rs7326277 |
GWAS Ctlg | rs7326277 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 24891316] Genetic variant in the 3'-untranslated region of VEGFR1 gene influences chronic obstructive pulmonary disease and lung cancer development in Chinese population