rs307821

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs307821(G;T)

Make rs307821(T;T)

Reference

GRCh38 38.1/142

Chromosome

5

Position

180603313

Gene

FLT4

is a	snp
is	mentioned by
dbSNP	rs307821
dbSNP (classic)	rs307821
ClinGen	rs307821
ebi	rs307821
HLI	rs307821
Exac	rs307821
Gnomad	rs307821
Varsome	rs307821
LitVar	rs307821
Map	rs307821
PheGenI	rs307821
Biobank	rs307821
1000 genomes	rs307821
hgdp	rs307821
ensembl	rs307821
geneview	rs307821
scholar	rs307821
google	rs307821
pharmgkb	rs307821
gwascentral	rs307821
openSNP	rs307821
23andMe	rs307821
SNPshot	rs307821
SNPdbe	rs307821
MSV3d	rs307821
GWAS Ctlg	rs307821

GMAF

0.05693

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 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	rs307821(A;A) rs307821(C;C) rs307821(T;T)
Alt	rs307821(A;A) rs307821(C;C) rs307821(T;T)
Reference	Rs307821(G;G)
Significance	Probable-non-pathogenic
Disease	not specified
Variation	info
Gene	FLT4
CLNDBN	not specified
Reversed	1
HGVS	NC_000005.9:g.180030313C>A; NC_000005.9:g.180030313C>G
CLNSRC
CLNACC	RCV000247350.1, RCV000242364.1,