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rs587776833

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AGA;AGA) 0 common in clinvar
(TCTC;TCTC) 0 common in clinvar
Make rs587776833(-;-)
Make rs587776833(-;AGA)
ReferenceGRCh38 38.1/142
Chromosome5
Position180614074
GeneFLT4
is asnp
is mentioned by
dbSNPrs587776833
ebirs587776833
HLIrs587776833
Exacrs587776833
Varsomers587776833
Maprs587776833
PheGenIrs587776833
hapmaprs587776833
1000 genomesrs587776833
hgdprs587776833
ensemblrs587776833
gopubmedrs587776833
geneviewrs587776833
scholarrs587776833
googlers587776833
pharmgkbrs587776833
gwascentralrs587776833
openSNPrs587776833
23andMers587776833
23andMe allrs587776833
SNP Nexus

SNPshotrs587776833
SNPdbers587776833
MSV3drs587776833
GWAS Ctlgrs587776833
Max Magnitude0
ClinVar
Risk rs587776833(AGAC,C;AGAC,C)
Alt rs587776833(AGAC,C;AGAC,C)
Reference rs587776833(TCTC;TCTC)
Significance Pathogenic
Disease Hereditary lymphedema type I
Variation info
Gene FLT4
CLNDBN Hereditary lymphedema type I
Reversed 1
HGVS NC_000005.9:g.180041074_180041076delAGA
CLNSRC OMIM Allelic Variant
CLNACC RCV000017656.28,