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rs121909650

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909650(C;C)
Make rs121909650(C;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position180616464
GeneFLT4
is asnp
is mentioned by
dbSNPrs121909650
ebirs121909650
HLIrs121909650
Exacrs121909650
Varsomers121909650
Maprs121909650
PheGenIrs121909650
hapmaprs121909650
1000 genomesrs121909650
hgdprs121909650
ensemblrs121909650
gopubmedrs121909650
geneviewrs121909650
scholarrs121909650
googlers121909650
pharmgkbrs121909650
gwascentralrs121909650
openSNPrs121909650
23andMers121909650
23andMe allrs121909650
SNP Nexus

SNPshotrs121909650
SNPdbers121909650
MSV3drs121909650
GWAS Ctlgrs121909650
Max Magnitude0
OMIM136352
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121909650(C;C)
Alt rs121909650(C;C)
Reference rs121909650(G;G)
Significance Pathogenic
Disease Hereditary lymphedema type I
Variation info
Gene FLT4
CLNDBN Hereditary lymphedema type I
Reversed 1
HGVS NC_000005.9:g.180043464C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000017648.24,