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rs34255532

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs34255532(C;T)
Make rs34255532(T;T)
ReferenceGRCh38 38.1/142
Chromosome5
Position180618911
GeneFLT4
is asnp
is mentioned by
dbSNPrs34255532
ebirs34255532
HLIrs34255532
Exacrs34255532
Varsomers34255532
Maprs34255532
PheGenIrs34255532
hapmaprs34255532
1000 genomesrs34255532
hgdprs34255532
ensemblrs34255532
gopubmedrs34255532
geneviewrs34255532
scholarrs34255532
googlers34255532
pharmgkbrs34255532
gwascentralrs34255532
openSNPrs34255532
23andMers34255532
23andMe allrs34255532
SNP Nexus

SNPshotrs34255532
SNPdbers34255532
MSV3drs34255532
GWAS Ctlgrs34255532
GMAF0.003214
Max Magnitude0
OMIM136352
Desc
Variant0007
Relatedalso


ClinVar
Risk rs34255532(T;T)
Alt rs34255532(T;T)
Reference rs34255532(C;C)
Significance Pathogenic
Disease Hemangioma
Variation info
Gene FLT4
CLNDBN Hemangioma, capillary infantile
Reversed 1
HGVS NC_000005.9:g.180045911G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017652.4,