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rs121909652

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909652(C;T)
Make rs121909652(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position180613101
GeneFLT4
is asnp
is mentioned by
dbSNPrs121909652
ebirs121909652
HLIrs121909652
Exacrs121909652
Varsomers121909652
Maprs121909652
PheGenIrs121909652
hapmaprs121909652
1000 genomesrs121909652
hgdprs121909652
ensemblrs121909652
gopubmedrs121909652
geneviewrs121909652
scholarrs121909652
googlers121909652
pharmgkbrs121909652
gwascentralrs121909652
openSNPrs121909652
23andMers121909652
23andMe allrs121909652
SNP Nexus

SNPshotrs121909652
SNPdbers121909652
MSV3drs121909652
GWAS Ctlgrs121909652
Max Magnitude0
OMIM136352
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121909652(T;T)
Alt rs121909652(T;T)
Reference rs121909652(C;C)
Significance Pathogenic
Disease Hereditary lymphedema type I
Variation info
Gene FLT4
CLNDBN Hereditary lymphedema type I
Reversed 1
HGVS NC_000005.9:g.180040101G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017650.28,