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rs448012

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs448012(C;C)
Make rs448012(C;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position180619344
GeneFLT4
is asnp
is mentioned by
dbSNPrs448012
dbSNP (classic)rs448012
ClinGenrs448012
ebirs448012
HLIrs448012
Exacrs448012
Gnomadrs448012
Varsomers448012
LitVarrs448012
Maprs448012
PheGenIrs448012
Biobankrs448012
1000 genomesrs448012
hgdprs448012
ensemblrs448012
geneviewrs448012
scholarrs448012
googlers448012
pharmgkbrs448012
gwascentralrs448012
openSNPrs448012
23andMers448012
SNPshotrs448012
SNPdbers448012
MSV3drs448012
GWAS Ctlgrs448012
GMAF0.4729
Max Magnitude0

[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,