rs587776610

Orientation

plus

Stabilized

plus

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

Make rs587776610(-;-)

Make rs587776610(-;GTT)

Reference

GRCh38 38.1/142

Chromosome

2

Position

144429800

Gene

ZEB2

is a	snp
is	mentioned by
dbSNP	rs587776610
dbSNP (classic)	rs587776610
ClinGen	rs587776610
ebi	rs587776610
HLI	rs587776610
Exac	rs587776610
Gnomad	rs587776610
Varsome	rs587776610
LitVar	rs587776610
Map	rs587776610
PheGenI	rs587776610
Biobank	rs587776610
1000 genomes	rs587776610
hgdp	rs587776610
ensembl	rs587776610
geneview	rs587776610
scholar	rs587776610
google	rs587776610
pharmgkb	rs587776610
gwascentral	rs587776610
openSNP	rs587776610
23andMe	rs587776610
SNPshot	rs587776610
SNPdbe	rs587776610
MSV3d	rs587776610
GWAS Ctlg	rs587776610

Max Magnitude

0

ClinVar
Risk	rs587776610(-;-)
Alt	rs587776610(-;-)
Reference	Rs587776610(GTT;GTT)
Significance	Pathogenic
Disease	Hirschsprung disease-mental retardation syndrome Mowat-Wilson syndrome
Variation	info
Gene	ZEB2
CLNDBN	Hirschsprung disease-mental retardation syndrome, late infantile Mowat-Wilson syndrome
Reversed	0
HGVS	NC_000002.11:g.145187367_145187369delGTT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000005030.2, RCV000490485.1,