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rs869025601

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869025601(C;T)
Make rs869025601(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position88715960
GeneMIR4722, PIEZO1
is asnp
is mentioned by
dbSNPrs869025601
ebirs869025601
HLIrs869025601
Exacrs869025601
Varsomers869025601
Maprs869025601
PheGenIrs869025601
hapmaprs869025601
1000 genomesrs869025601
hgdprs869025601
ensemblrs869025601
gopubmedrs869025601
geneviewrs869025601
scholarrs869025601
googlers869025601
pharmgkbrs869025601
gwascentralrs869025601
openSNPrs869025601
23andMers869025601
23andMe allrs869025601
SNP Nexus

SNPshotrs869025601
SNPdbers869025601
MSV3drs869025601
GWAS Ctlgrs869025601
Max Magnitude0
ClinVar
Risk rs869025601(T;T)
Alt rs869025601(T;T)
Reference rs869025601(C;C)
Significance Pathogenic
Disease Lymphedema
Variation info
Gene MIR4722 PIEZO1
CLNDBN Lymphedema, hereditary, III
Reversed 1
HGVS NC_000016.9:g.88782368G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000208773.2,