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rs121909657

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909657(A;A)
Make rs121909657(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position180619749
GeneFLT4
is asnp
is mentioned by
dbSNPrs121909657
ebirs121909657
HLIrs121909657
Exacrs121909657
Varsomers121909657
Maprs121909657
PheGenIrs121909657
hapmaprs121909657
1000 genomesrs121909657
hgdprs121909657
ensemblrs121909657
gopubmedrs121909657
geneviewrs121909657
scholarrs121909657
googlers121909657
pharmgkbrs121909657
gwascentralrs121909657
openSNPrs121909657
23andMers121909657
23andMe allrs121909657
SNP Nexus

SNPshotrs121909657
SNPdbers121909657
MSV3drs121909657
GWAS Ctlgrs121909657
GMAF0.0004591
Max Magnitude0
OMIM136352
Desc
Variant0012
Relatedalso
ClinVar
Risk rs121909657(A;A)
Alt rs121909657(A;A)
Reference rs121909657(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.180046749C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017657.28,