rs34255532

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in complete genomics

Make rs34255532(C;T)

Make rs34255532(T;T)

Reference

GRCh38 38.1/142

Chromosome

5

Position

180618911

Gene

FLT4

is a	snp
is	mentioned by
dbSNP	rs34255532
dbSNP (classic)	rs34255532
ClinGen	rs34255532
ebi	rs34255532
HLI	rs34255532
Exac	rs34255532
Gnomad	rs34255532
Varsome	rs34255532
LitVar	rs34255532
Map	rs34255532
PheGenI	rs34255532
Biobank	rs34255532
1000 genomes	rs34255532
hgdp	rs34255532
ensembl	rs34255532
geneview	rs34255532
scholar	rs34255532
google	rs34255532
pharmgkb	rs34255532
gwascentral	rs34255532
openSNP	rs34255532
23andMe	rs34255532
SNPshot	rs34255532
SNPdbe	rs34255532
MSV3d	rs34255532
GWAS Ctlg	rs34255532

GMAF

0.003214

Max Magnitude

0

OMIM	136352
Desc
Variant	0007
Related	also

ClinVar
Risk	rs34255532(T;T)
Alt	rs34255532(T;T)
Reference	Rs34255532(C;C)
Significance	Pathogenic
Disease	Hemangioma not specified
Variation	info
Gene	FLT4
CLNDBN	Hemangioma, capillary infantile not specified
Reversed	1
HGVS	NC_000005.9:g.180045911G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017652.4, RCV000249222.1,