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rs370296725

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs370296725(C;T)
Make rs370296725(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position88717172
GeneMIR4722, PIEZO1
is asnp
is mentioned by
dbSNPrs370296725
dbSNP (classic)rs370296725
ClinGenrs370296725
ebirs370296725
HLIrs370296725
Exacrs370296725
Gnomadrs370296725
Varsomers370296725
LitVarrs370296725
Maprs370296725
PheGenIrs370296725
Biobankrs370296725
1000 genomesrs370296725
hgdprs370296725
ensemblrs370296725
geneviewrs370296725
scholarrs370296725
googlers370296725
pharmgkbrs370296725
gwascentralrs370296725
openSNPrs370296725
23andMers370296725
SNPshotrs370296725
SNPdbers370296725
MSV3drs370296725
GWAS Ctlgrs370296725
Max Magnitude0
ClinVar
Risk rs370296725(A;A) rs370296725(T;T)
Alt rs370296725(A;A) rs370296725(T;T)
Reference Rs370296725(C;C)
Significance Pathogenic
Disease Lymphedema
Variation info
Gene MIR4722 PIEZO1
CLNDBN Lymphedema, hereditary, III
Reversed 0
HGVS NC_000016.9:g.88783580C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000208749.2,