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rs587777764

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777764(A;A)
Make rs587777764(A;G)
ReferenceGRCh38 38.1/142
Chromosome16
Position88720174
GenePIEZO1
is asnp
is mentioned by
dbSNPrs587777764
ebirs587777764
HLIrs587777764
Exacrs587777764
Varsomers587777764
Maprs587777764
PheGenIrs587777764
hapmaprs587777764
1000 genomesrs587777764
hgdprs587777764
ensemblrs587777764
gopubmedrs587777764
geneviewrs587777764
scholarrs587777764
googlers587777764
pharmgkbrs587777764
gwascentralrs587777764
openSNPrs587777764
23andMers587777764
23andMe allrs587777764
SNP Nexus

SNPshotrs587777764
SNPdbers587777764
MSV3drs587777764
GWAS Ctlgrs587777764
Max Magnitude0
ClinVar
Risk rs587777764(A;A)
Alt rs587777764(A;A)
Reference rs587777764(G;G)
Significance Pathogenic
Disease Xerocytosis
Variation info
Gene PIEZO1
CLNDBN Xerocytosis
Reversed 0
HGVS NC_000016.9:g.88786582G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000049235.3,