rs121909654

Orientation

minus

Stabilized

minus

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

Make rs121909654(A;A)

Make rs121909654(A;G)

Reference

GRCh38 38.1/141

Chromosome

5

Position

180619680

Gene

FLT4

is a	snp
is	mentioned by
dbSNP	rs121909654
dbSNP (classic)	rs121909654
ClinGen	rs121909654
ebi	rs121909654
HLI	rs121909654
Exac	rs121909654
Gnomad	rs121909654
Varsome	rs121909654
LitVar	rs121909654
Map	rs121909654
PheGenI	rs121909654
Biobank	rs121909654
1000 genomes	rs121909654
hgdp	rs121909654
ensembl	rs121909654
geneview	rs121909654
scholar	rs121909654
google	rs121909654
pharmgkb	rs121909654
gwascentral	rs121909654
openSNP	rs121909654
23andMe	rs121909654
SNPshot	rs121909654
SNPdbe	rs121909654
MSV3d	rs121909654
GWAS Ctlg	rs121909654

Max Magnitude

0

OMIM	136352
Desc
Variant	0008
Related	also

ClinVar
Risk	rs121909654(A;A)
Alt	rs121909654(A;A)
Reference	Rs121909654(G;G)
Significance	Pathogenic
Disease	Hereditary lymphedema type I
Variation	info
Gene	FLT4
CLNDBN	Hereditary lymphedema type I
Reversed	1
HGVS	NC_000005.9:g.180046680C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017653.28,