Have questions? Visit https://www.reddit.com/r/SNPedia

rs121909656

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909656(A;A)
Make rs121909656(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position180614083
GeneFLT4
is asnp
is mentioned by
dbSNPrs121909656
ebirs121909656
HLIrs121909656
Exacrs121909656
Varsomers121909656
Maprs121909656
PheGenIrs121909656
hapmaprs121909656
1000 genomesrs121909656
hgdprs121909656
ensemblrs121909656
gopubmedrs121909656
geneviewrs121909656
scholarrs121909656
googlers121909656
pharmgkbrs121909656
gwascentralrs121909656
openSNPrs121909656
23andMers121909656
23andMe allrs121909656
SNP Nexus

SNPshotrs121909656
SNPdbers121909656
MSV3drs121909656
GWAS Ctlgrs121909656
Max Magnitude0
OMIM136352
Desc
Variant0010
Relatedalso
ClinVar
Risk rs121909656(A;A)
Alt rs121909656(A;A)
Reference rs121909656(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.180041083C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017655.28,