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rs121909653

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121909653(A;G)
Make rs121909653(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position180616482
GeneFLT4
is asnp
is mentioned by
dbSNPrs121909653
ebirs121909653
HLIrs121909653
Exacrs121909653
Varsomers121909653
Maprs121909653
PheGenIrs121909653
hapmaprs121909653
1000 genomesrs121909653
hgdprs121909653
ensemblrs121909653
gopubmedrs121909653
geneviewrs121909653
scholarrs121909653
googlers121909653
pharmgkbrs121909653
gwascentralrs121909653
openSNPrs121909653
23andMers121909653
23andMe allrs121909653
SNP Nexus

SNPshotrs121909653
SNPdbers121909653
MSV3drs121909653
GWAS Ctlgrs121909653
Max Magnitude0
OMIM136352
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121909653(G;G)
Alt rs121909653(G;G)
Reference rs121909653(A;A)
Significance Pathogenic
Disease Hereditary lymphedema type I
Variation info
Gene FLT4
CLNDBN Hereditary lymphedema type I
Reversed 1
HGVS NC_000005.9:g.180043482T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000017651.28,