rs121917766

Orientation

minus

Stabilized

minus

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

Make rs121917766(C;T)

Make rs121917766(T;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

55088939

Gene

KDR

is a	snp
is	mentioned by
dbSNP	rs121917766
dbSNP (classic)	rs121917766
ClinGen	rs121917766
ebi	rs121917766
HLI	rs121917766
Exac	rs121917766
Gnomad	rs121917766
Varsome	rs121917766
LitVar	rs121917766
Map	rs121917766
PheGenI	rs121917766
Biobank	rs121917766
1000 genomes	rs121917766
hgdp	rs121917766
ensembl	rs121917766
geneview	rs121917766
scholar	rs121917766
google	rs121917766
pharmgkb	rs121917766
gwascentral	rs121917766
openSNP	rs121917766
23andMe	rs121917766
SNPshot	rs121917766
SNPdbe	rs121917766
MSV3d	rs121917766
GWAS Ctlg	rs121917766

Max Magnitude

0

OMIM	191306
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121917766(T;T)
Alt	rs121917766(T;T)
Reference	Rs121917766(C;C)
Significance	Pathogenic
Disease	Hemangioma not specified
Variation	info
Gene	KDR
CLNDBN	Hemangioma, capillary infantile not specified
Reversed	1
HGVS	NC_000004.11:g.55955106G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013110.4, RCV000121300.1,