rs2296189

Orientation

plus

Stabilized

plus

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

Make rs2296189(A;G)

Make rs2296189(G;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

28319505

Gene

FLT1

is a	snp
is	mentioned by
dbSNP	rs2296189
dbSNP (classic)	rs2296189
ClinGen	rs2296189
ebi	rs2296189
HLI	rs2296189
Exac	rs2296189
Gnomad	rs2296189
Varsome	rs2296189
LitVar	rs2296189
Map	rs2296189
PheGenI	rs2296189
Biobank	rs2296189
1000 genomes	rs2296189
hgdp	rs2296189
ensembl	rs2296189
geneview	rs2296189
scholar	rs2296189
google	rs2296189
pharmgkb	rs2296189
gwascentral	rs2296189
openSNP	rs2296189
23andMe	rs2296189
SNPshot	rs2296189
SNPdbe	rs2296189
MSV3d	rs2296189
GWAS Ctlg	rs2296189

GMAF

0.1763

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

[PMID 23794399] VEGFA, FLT1, KDR and colorectal cancer: Assessment of disease risk, tumor molecular phenotype, and survival

ClinVar
Risk	rs2296189(C;C) rs2296189(G;G)
Alt	rs2296189(C;C) rs2296189(G;G)
Reference	Rs2296189(A;A)
Significance	Untested
Disease	Carcinoma of colon
Variation	info
Gene	FLT1
CLNDBN	Carcinoma of colon
Reversed	0
HGVS	NC_000013.10:g.28893642A>G
CLNSRC	ClinVar
CLNACC	RCV000149490.1,