rs6838834
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs6838834(C;T) |
Make rs6838834(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 176732444 |
Gene | VEGFC |
is a | snp |
is | mentioned by |
dbSNP | rs6838834 |
dbSNP (classic) | rs6838834 |
ClinGen | rs6838834 |
ebi | rs6838834 |
HLI | rs6838834 |
Exac | rs6838834 |
Gnomad | rs6838834 |
Varsome | rs6838834 |
LitVar | rs6838834 |
Map | rs6838834 |
PheGenI | rs6838834 |
Biobank | rs6838834 |
1000 genomes | rs6838834 |
hgdp | rs6838834 |
ensembl | rs6838834 |
geneview | rs6838834 |
scholar | rs6838834 |
rs6838834 | |
pharmgkb | rs6838834 |
gwascentral | rs6838834 |
openSNP | rs6838834 |
23andMe | rs6838834 |
SNPshot | rs6838834 |
SNPdbe | rs6838834 |
MSV3d | rs6838834 |
GWAS Ctlg | rs6838834 |
GMAF | 0.03352 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 20223440] Allelic variations in angiogenic pathway genes are associated with preeclampsia