Have questions? Visit https://www.reddit.com/r/SNPedia

rs587776987

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(T;T) 0 common in clinvar
Make rs587776987(A;C)
Make rs587776987(C;C)
ReferenceGRCh38 38.1/142
Chromosome16
Position88716885
GeneMIR4722, PIEZO1
is asnp
is mentioned by
dbSNPrs587776987
ebirs587776987
HLIrs587776987
Exacrs587776987
Varsomers587776987
Maprs587776987
PheGenIrs587776987
hapmaprs587776987
1000 genomesrs587776987
hgdprs587776987
ensemblrs587776987
gopubmedrs587776987
geneviewrs587776987
scholarrs587776987
googlers587776987
pharmgkbrs587776987
gwascentralrs587776987
openSNPrs587776987
23andMers587776987
23andMe allrs587776987
SNP Nexus

SNPshotrs587776987
SNPdbers587776987
MSV3drs587776987
GWAS Ctlgrs587776987
Max Magnitude0
ClinVar
Risk rs587776987(A,C;A,C)
Alt rs587776987(A,C;A,C)
Reference rs587776987(T;T)
Significance Pathogenic
Disease Xerocytosis
Variation info
Gene MIR4722 PIEZO1
CLNDBN Xerocytosis
Reversed 1
HGVS NC_000016.9:g.88783293A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000049231.5,