rs121909652

Orientation

minus

Stabilized

minus

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

Make rs121909652(C;T)

Make rs121909652(T;T)

Reference

GRCh38 38.1/141

Chromosome

5

Position

180613101

Gene

FLT4

is a	snp
is	mentioned by
dbSNP	rs121909652
dbSNP (classic)	rs121909652
ClinGen	rs121909652
ebi	rs121909652
HLI	rs121909652
Exac	rs121909652
Gnomad	rs121909652
Varsome	rs121909652
LitVar	rs121909652
Map	rs121909652
PheGenI	rs121909652
Biobank	rs121909652
1000 genomes	rs121909652
hgdp	rs121909652
ensembl	rs121909652
geneview	rs121909652
scholar	rs121909652
google	rs121909652
pharmgkb	rs121909652
gwascentral	rs121909652
openSNP	rs121909652
23andMe	rs121909652
SNPshot	rs121909652
SNPdbe	rs121909652
MSV3d	rs121909652
GWAS Ctlg	rs121909652

Max Magnitude

0

OMIM	136352
Desc
Variant	0005
Related	also

ClinVar
Risk	rs121909652(T;T)
Alt	rs121909652(T;T)
Reference	Rs121909652(C;C)
Significance	Pathogenic
Disease	Hereditary lymphedema type I
Variation	info
Gene	FLT4
CLNDBN	Hereditary lymphedema type I
Reversed	1
HGVS	NC_000005.9:g.180040101G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017650.28,