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rs121909654

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909654(A;A)
Make rs121909654(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position180619680
GeneFLT4
is asnp
is mentioned by
dbSNPrs121909654
ebirs121909654
HLIrs121909654
Exacrs121909654
Varsomers121909654
Maprs121909654
PheGenIrs121909654
hapmaprs121909654
1000 genomesrs121909654
hgdprs121909654
ensemblrs121909654
gopubmedrs121909654
geneviewrs121909654
scholarrs121909654
googlers121909654
pharmgkbrs121909654
gwascentralrs121909654
openSNPrs121909654
23andMers121909654
23andMe allrs121909654
SNP Nexus

SNPshotrs121909654
SNPdbers121909654
MSV3drs121909654
GWAS Ctlgrs121909654
Max Magnitude0
OMIM136352
Desc
Variant0008
Relatedalso
ClinVar
Risk rs121909654(A;A)
Alt rs121909654(A;A)
Reference rs121909654(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.180046680C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017653.28,