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rs587776988

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587776988(C;T)
Make rs587776988(T;T)
ReferenceGRCh38 38.1/142
Chromosome16
Position88715804
GeneCTU2, MIR4722, PIEZO1
is asnp
is mentioned by
dbSNPrs587776988
ebirs587776988
HLIrs587776988
Exacrs587776988
Varsomers587776988
Maprs587776988
PheGenIrs587776988
hapmaprs587776988
1000 genomesrs587776988
hgdprs587776988
ensemblrs587776988
gopubmedrs587776988
geneviewrs587776988
scholarrs587776988
googlers587776988
pharmgkbrs587776988
gwascentralrs587776988
openSNPrs587776988
23andMers587776988
23andMe allrs587776988
SNP Nexus

SNPshotrs587776988
SNPdbers587776988
MSV3drs587776988
GWAS Ctlgrs587776988
Max Magnitude0
ClinVar
Risk rs587776988(C,T;C,T)
Alt rs587776988(C,T;C,T)
Reference rs587776988(G;G)
Significance Pathogenic
Disease Xerocytosis
Variation info
Gene CTU2 MIR4722 PIEZO1
CLNDBN Xerocytosis
Reversed 1
HGVS NC_000016.9:g.88782212C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000049232.5,