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rs587777725

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777725(-;-)
Make rs587777725(-;C)
ReferenceGRCh38 38.1/142
Chromosome4
Position125317606
GeneFAT4
is asnp
is mentioned by
dbSNPrs587777725
ebirs587777725
HLIrs587777725
Exacrs587777725
Varsomers587777725
Maprs587777725
PheGenIrs587777725
hapmaprs587777725
1000 genomesrs587777725
hgdprs587777725
ensemblrs587777725
gopubmedrs587777725
geneviewrs587777725
scholarrs587777725
googlers587777725
pharmgkbrs587777725
gwascentralrs587777725
openSNPrs587777725
23andMers587777725
23andMe allrs587777725
SNP Nexus

SNPshotrs587777725
SNPdbers587777725
MSV3drs587777725
GWAS Ctlgrs587777725
Max Magnitude0
ClinVar
Risk rs587777725(;)
Alt rs587777725(;)
Reference rs587777725(C;C)
Significance Pathogenic
Disease Hennekam lymphangiectasia-lymphedema syndrome 2
Variation info
Gene FAT4
CLNDBN Hennekam lymphangiectasia-lymphedema syndrome 2
Reversed 0
HGVS NC_000004.11:g.126238761delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000144159.3,