rs587776987

Orientation

plus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common in clinvar
(T;T)	0	common in clinvar

Make rs587776987(A;C)

Make rs587776987(C;C)

Reference

GRCh38 38.1/142

Chromosome

16

Position

88716885

Gene	MIR4722, PIEZO1

is a	snp
is	mentioned by
dbSNP	rs587776987
dbSNP (classic)	rs587776987
ClinGen	rs587776987
ebi	rs587776987
HLI	rs587776987
Exac	rs587776987
Gnomad	rs587776987
Varsome	rs587776987
LitVar	rs587776987
Map	rs587776987
PheGenI	rs587776987
Biobank	rs587776987
1000 genomes	rs587776987
hgdp	rs587776987
ensembl	rs587776987
geneview	rs587776987
scholar	rs587776987
google	rs587776987
pharmgkb	rs587776987
gwascentral	rs587776987
openSNP	rs587776987
23andMe	rs587776987
SNPshot	rs587776987
SNPdbe	rs587776987
MSV3d	rs587776987
GWAS Ctlg	rs587776987

Max Magnitude

0

ClinVar
Risk	Rs587776987(A;A) rs587776987(C;C)
Alt	Rs587776987(A;A) rs587776987(C;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 UniProtKB (protein)
CLNACC	RCV000049231.5,