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rs587777567

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777567(A;A)
Make rs587777567(A;G)
ReferenceGRCh38 38.1/142
Chromosome4
Position176711575
GeneVEGFC
is asnp
is mentioned by
dbSNPrs587777567
ebirs587777567
HLIrs587777567
Exacrs587777567
Varsomers587777567
Maprs587777567
PheGenIrs587777567
hapmaprs587777567
1000 genomesrs587777567
hgdprs587777567
ensemblrs587777567
gopubmedrs587777567
geneviewrs587777567
scholarrs587777567
googlers587777567
pharmgkbrs587777567
gwascentralrs587777567
openSNPrs587777567
23andMers587777567
23andMe allrs587777567
SNP Nexus

SNPshotrs587777567
SNPdbers587777567
MSV3drs587777567
GWAS Ctlgrs587777567
Max Magnitude0
ClinVar
Risk rs587777567(A;A)
Alt rs587777567(A;A)
Reference rs587777567(G;G)
Significance Pathogenic
Disease Lymphedema
Variation info
Gene VEGFC
CLNDBN Lymphedema, hereditary, ID
Reversed 0
HGVS NC_000004.11:g.177632729G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000128849.3,