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rs121917766

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121917766(C;T)
Make rs121917766(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position55088939
GeneKDR
is asnp
is mentioned by
dbSNPrs121917766
ebirs121917766
HLIrs121917766
Exacrs121917766
Varsomers121917766
Maprs121917766
PheGenIrs121917766
hapmaprs121917766
1000 genomesrs121917766
hgdprs121917766
ensemblrs121917766
gopubmedrs121917766
geneviewrs121917766
scholarrs121917766
googlers121917766
pharmgkbrs121917766
gwascentralrs121917766
openSNPrs121917766
23andMers121917766
23andMe allrs121917766
SNP Nexus

SNPshotrs121917766
SNPdbers121917766
MSV3drs121917766
GWAS Ctlgrs121917766
Max Magnitude0
OMIM191306
Desc
Variant0001
Relatedalso
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
CLNACC RCV000013110.4, RCV000121300.1,