rs448012
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs448012(C;C) |
Make rs448012(C;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 180619344 |
Gene | FLT4 |
is a | snp |
is | mentioned by |
dbSNP | rs448012 |
dbSNP (classic) | rs448012 |
ClinGen | rs448012 |
ebi | rs448012 |
HLI | rs448012 |
Exac | rs448012 |
Gnomad | rs448012 |
Varsome | rs448012 |
LitVar | rs448012 |
Map | rs448012 |
PheGenI | rs448012 |
Biobank | rs448012 |
1000 genomes | rs448012 |
hgdp | rs448012 |
ensembl | rs448012 |
geneview | rs448012 |
scholar | rs448012 |
rs448012 | |
pharmgkb | rs448012 |
gwascentral | rs448012 |
openSNP | rs448012 |
23andMe | rs448012 |
SNPshot | rs448012 |
SNPdbe | rs448012 |
MSV3d | rs448012 |
GWAS Ctlg | rs448012 |
GMAF | 0.4729 |
Max Magnitude | 0 |
[PMID 22015057] Single nucleotide polymorphism associations with response and toxic effects in patients with advanced renal-cell carcinoma treated with first-line sunitinib: a multicentre, observational, prospective study
[PMID 25239121] Variants in angiogenesis-related genes and the risk of clear cell renal cell carcinoma
ClinVar | |
---|---|
Risk | rs448012(C;C) |
Alt | rs448012(C;C) |
Reference | Rs448012(G;G) |
Significance | Non-pathogenic |
Disease | not specified |
Variation | info |
Gene | FLT4 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000005.9:g.180046344G>C |
CLNSRC | |
CLNACC | RCV000251871.1, |