rs587776992

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	0	common in clinvar

Make rs587776992(-;AGCTCC)

Make rs587776992(AGCTCC;AGCTCC)

Reference

GRCh38 38.1/142

Chromosome

16

Position

88715692

Gene	CTU2, PIEZO1

is a	snp
is	mentioned by
dbSNP	rs587776992
dbSNP (classic)	rs587776992
ClinGen	rs587776992
ebi	rs587776992
HLI	rs587776992
Exac	rs587776992
Gnomad	rs587776992
Varsome	rs587776992
LitVar	rs587776992
Map	rs587776992
PheGenI	rs587776992
Biobank	rs587776992
1000 genomes	rs587776992
hgdp	rs587776992
ensembl	rs587776992
geneview	rs587776992
scholar	rs587776992
google	rs587776992
pharmgkb	rs587776992
gwascentral	rs587776992
openSNP	rs587776992
23andMe	rs587776992
SNPshot	rs587776992
SNPdbe	rs587776992
MSV3d	rs587776992
GWAS Ctlg	rs587776992

Max Magnitude

0

ClinVar
Risk	rs587776992(CTCCAG;CTCCAG)
Alt	rs587776992(CTCCAG;CTCCAG)
Reference	Rs587776992(-;-)
Significance	Pathogenic
Disease	Xerocytosis not provided
Variation	info
Gene	CTU2 PIEZO1
CLNDBN	Xerocytosis not provided
Reversed	0
HGVS	NC_000016.9:g.88782091_88782096dupCTCCAG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000049237.4, RCV000485661.1,