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rs587777766

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777766(C;C)
Make rs587777766(C;G)
ReferenceGRCh38 38.1/142
Chromosome16
Position88734844
GenePIEZO1, RP5-1142A6.2
is asnp
is mentioned by
dbSNPrs587777766
ebirs587777766
HLIrs587777766
Exacrs587777766
Varsomers587777766
Maprs587777766
PheGenIrs587777766
hapmaprs587777766
1000 genomesrs587777766
hgdprs587777766
ensemblrs587777766
gopubmedrs587777766
geneviewrs587777766
scholarrs587777766
googlers587777766
pharmgkbrs587777766
gwascentralrs587777766
openSNPrs587777766
23andMers587777766
23andMe allrs587777766
SNP Nexus

SNPshotrs587777766
SNPdbers587777766
MSV3drs587777766
GWAS Ctlgrs587777766
Max Magnitude0
ClinVar
Risk rs587777766(C;C)
Alt rs587777766(C;C)
Reference rs587777766(G;G)
Significance Pathogenic
Disease Xerocytosis
Variation info
Gene LOC100289580 PIEZO1
CLNDBN Xerocytosis
Reversed 0
HGVS NC_000016.9:g.88801252G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000049238.1,