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rs869025598

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869025598(C;T)
Make rs869025598(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position88716877
GeneMIR4722, PIEZO1
is asnp
is mentioned by
dbSNPrs869025598
ebirs869025598
HLIrs869025598
Exacrs869025598
Varsomers869025598
Maprs869025598
PheGenIrs869025598
hapmaprs869025598
1000 genomesrs869025598
hgdprs869025598
ensemblrs869025598
gopubmedrs869025598
geneviewrs869025598
scholarrs869025598
googlers869025598
pharmgkbrs869025598
gwascentralrs869025598
openSNPrs869025598
23andMers869025598
23andMe allrs869025598
SNP Nexus

SNPshotrs869025598
SNPdbers869025598
MSV3drs869025598
GWAS Ctlgrs869025598
Max Magnitude0
ClinVar
Risk rs869025598(T;T)
Alt rs869025598(T;T)
Reference rs869025598(C;C)
Significance Pathogenic
Disease Lymphedema
Variation info
Gene MIR4722 PIEZO1
CLNDBN Lymphedema, hereditary, III
Reversed 1
HGVS NC_000016.9:g.88783285G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000208759.2,