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rs267606818

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606818(A;A)
Make rs267606818(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position180619743
GeneFLT4
is asnp
is mentioned by
dbSNPrs267606818
ebirs267606818
HLIrs267606818
Exacrs267606818
Varsomers267606818
Maprs267606818
PheGenIrs267606818
hapmaprs267606818
1000 genomesrs267606818
hgdprs267606818
ensemblrs267606818
gopubmedrs267606818
geneviewrs267606818
scholarrs267606818
googlers267606818
pharmgkbrs267606818
gwascentralrs267606818
openSNPrs267606818
23andMers267606818
23andMe allrs267606818
SNP Nexus

SNPshotrs267606818
SNPdbers267606818
MSV3drs267606818
GWAS Ctlgrs267606818
Max Magnitude0
ClinVar
Risk rs267606818(A;A)
Alt rs267606818(A;A)
Reference rs267606818(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.180046743C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017647.28,