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rs121909655

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121909655(C;C)
Make rs121909655(C;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position180614142
GeneFLT4
is asnp
is mentioned by
dbSNPrs121909655
ebirs121909655
HLIrs121909655
Exacrs121909655
Varsomers121909655
Maprs121909655
PheGenIrs121909655
hapmaprs121909655
1000 genomesrs121909655
hgdprs121909655
ensemblrs121909655
gopubmedrs121909655
geneviewrs121909655
scholarrs121909655
googlers121909655
pharmgkbrs121909655
gwascentralrs121909655
openSNPrs121909655
23andMers121909655
23andMe allrs121909655
SNP Nexus

SNPshotrs121909655
SNPdbers121909655
MSV3drs121909655
GWAS Ctlgrs121909655
Max Magnitude0
OMIM136352
Desc
Variant0009
Relatedalso
ClinVar
Risk rs121909655(C;C)
Alt rs121909655(C;C)
Reference rs121909655(T;T)
Significance Pathogenic
Disease Hereditary lymphedema type I
Variation info
Gene FLT4
CLNDBN Hereditary lymphedema type I
Reversed 1
HGVS NC_000005.9:g.180041142A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000017654.28,