rs587776988

Orientation

plus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(G;G)	0	common in clinvar

Make rs587776988(C;T)

Make rs587776988(T;T)

Reference

GRCh38 38.1/142

Chromosome

16

Position

88715804

Gene	CTU2, MIR4722, PIEZO1

is a	snp
is	mentioned by
dbSNP	rs587776988
dbSNP (classic)	rs587776988
ClinGen	rs587776988
ebi	rs587776988
HLI	rs587776988
Exac	rs587776988
Gnomad	rs587776988
Varsome	rs587776988
LitVar	rs587776988
Map	rs587776988
PheGenI	rs587776988
Biobank	rs587776988
1000 genomes	rs587776988
hgdp	rs587776988
ensembl	rs587776988
geneview	rs587776988
scholar	rs587776988
google	rs587776988
pharmgkb	rs587776988
gwascentral	rs587776988
openSNP	rs587776988
23andMe	rs587776988
SNPshot	rs587776988
SNPdbe	rs587776988
MSV3d	rs587776988
GWAS Ctlg	rs587776988

Max Magnitude

0

ClinVar
Risk	Rs587776988(C;C) rs587776988(T;T)
Alt	Rs587776988(C;C) rs587776988(T;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 UniProtKB (protein)
CLNACC	RCV000049232.5,