rs307826

minus

Geno	Mag	Summary
(A;A)	0	common on affy axiom data

Make rs307826(A;G)

Make rs307826(G;G)

Reference

GRCh38 38.1/141

Chromosome

5

Position

180624003

Gene

FLT4

is a	snp
is	mentioned by
dbSNP	rs307826
dbSNP (classic)	rs307826
ClinGen	rs307826
ebi	rs307826
HLI	rs307826
Exac	rs307826
Gnomad	rs307826
Varsome	rs307826
LitVar	rs307826
Map	rs307826
PheGenI	rs307826
Biobank	rs307826
1000 genomes	rs307826
hgdp	rs307826
ensembl	rs307826
geneview	rs307826
scholar	rs307826
google	rs307826
pharmgkb	rs307826
gwascentral	rs307826
openSNP	rs307826
23andMe	rs307826
SNPshot	rs307826
SNPdbe	rs307826
MSV3d	rs307826
GWAS Ctlg	rs307826

GMAF

0.05234

Max Magnitude

0

?

(A;A) (A;G) (G;G)

28

[PMID 20223440] Allelic variations in angiogenic pathway genes are associated with preeclampsia

[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 23788753] Prospective study assessing hypoxia-related proteins as markers for the outcome of treatment with sunitinib in advanced clear-cell renal cell carcinoma

[PMID 23462807 ] Single-nucleotide polymorphisms associated with outcome in metastatic renal cell carcinoma treated with sunitinib.

[PMID 26254278 ] Impact of VEGF, VEGFR, PDGFR, HIF and ERCC1 gene polymorphisms on thymic malignancies outcome after thymectomy

ClinVar
Risk	rs307826(G;G) rs307826(T;T)
Alt	rs307826(G;G) rs307826(T;T)
Reference	Rs307826(A;A)
Significance	Non-pathogenic
Disease	not specified
Variation	info
Gene	FLT4
CLNDBN	not specified
Reversed	1
HGVS	NC_000005.9:g.180051003T>C
CLNSRC
CLNACC	RCV000254379.1,