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rs587776992

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587776992(-;-)
Make rs587776992(-;AGCTCC)
Make rs587776992(AGCTCC;AGCTCC)
ReferenceGRCh38 38.1/142
Chromosome16
Position88715692
GeneCTU2, PIEZO1
is asnp
is mentioned by
dbSNPrs587776992
ebirs587776992
HLIrs587776992
Exacrs587776992
Varsomers587776992
Maprs587776992
PheGenIrs587776992
hapmaprs587776992
1000 genomesrs587776992
hgdprs587776992
ensemblrs587776992
gopubmedrs587776992
geneviewrs587776992
scholarrs587776992
googlers587776992
pharmgkbrs587776992
gwascentralrs587776992
openSNPrs587776992
23andMers587776992
23andMe allrs587776992
SNP Nexus

SNPshotrs587776992
SNPdbers587776992
MSV3drs587776992
GWAS Ctlgrs587776992
Max Magnitude0
ClinVar
Risk rs587776992(CTCCAG;CTCCAG)
Alt rs587776992(CTCCAG;CTCCAG)
Reference rs587776992(;)
Significance Pathogenic
Disease Xerocytosis
Variation info
Gene CTU2 PIEZO1
CLNDBN Xerocytosis
Reversed 0
HGVS NC_000016.9:g.88782095_88782100dupAGCTCC
CLNSRC OMIM Allelic Variant
CLNACC RCV000049237.4,