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rs587777765

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777765(A;A)
Make rs587777765(A;G)
ReferenceGRCh38 38.1/142
Chromosome16
Position88727144
GenePIEZO1
is asnp
is mentioned by
dbSNPrs587777765
ebirs587777765
HLIrs587777765
Exacrs587777765
Varsomers587777765
Maprs587777765
PheGenIrs587777765
hapmaprs587777765
1000 genomesrs587777765
hgdprs587777765
ensemblrs587777765
gopubmedrs587777765
geneviewrs587777765
scholarrs587777765
googlers587777765
pharmgkbrs587777765
gwascentralrs587777765
openSNPrs587777765
23andMers587777765
23andMe allrs587777765
SNP Nexus

SNPshotrs587777765
SNPdbers587777765
MSV3drs587777765
GWAS Ctlgrs587777765
Max Magnitude0
ClinVar
Risk rs587777765(A;A)
Alt rs587777765(A;A)
Reference rs587777765(G;G)
Significance Pathogenic
Disease Xerocytosis
Variation info
Gene PIEZO1
CLNDBN Xerocytosis
Reversed 0
HGVS NC_000016.9:g.88793552G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000049235.3,