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rs121909651

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121909651(C;C)
Make rs121909651(C;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position180616455
GeneFLT4
is asnp
is mentioned by
dbSNPrs121909651
ebirs121909651
HLIrs121909651
Exacrs121909651
Varsomers121909651
Maprs121909651
PheGenIrs121909651
hapmaprs121909651
1000 genomesrs121909651
hgdprs121909651
ensemblrs121909651
gopubmedrs121909651
geneviewrs121909651
scholarrs121909651
googlers121909651
pharmgkbrs121909651
gwascentralrs121909651
openSNPrs121909651
23andMers121909651
23andMe allrs121909651
SNP Nexus

SNPshotrs121909651
SNPdbers121909651
MSV3drs121909651
GWAS Ctlgrs121909651
Max Magnitude0
OMIM136352
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121909651(C;C)
Alt rs121909651(C;C)
Reference rs121909651(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.180043455A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000017649.28,