rs267608593

Orientation

minus

Stabilized

minus

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

Make rs267608593(-;-)

Make rs267608593(-;CCCCACCTCCACCTGAGCCCGAGAGCTCC)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154030640

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608593
dbSNP (classic)	rs267608593
ClinGen	rs267608593
ebi	rs267608593
HLI	rs267608593
Exac	rs267608593
Gnomad	rs267608593
Varsome	rs267608593
LitVar	rs267608593
Map	rs267608593
PheGenI	rs267608593
Biobank	rs267608593
1000 genomes	rs267608593
hgdp	rs267608593
ensembl	rs267608593
geneview	rs267608593
scholar	rs267608593
google	rs267608593
pharmgkb	rs267608593
gwascentral	rs267608593
openSNP	rs267608593
23andMe	rs267608593
SNPshot	rs267608593
SNPdbe	rs267608593
MSV3d	rs267608593
GWAS Ctlg	rs267608593

Max Magnitude

0

ClinVar
Risk	rs267608593(-;-)
Alt	rs267608593(-;-)
Reference	Rs267608593(CCCCACCTCCACCTGAGCCCGAGAGCTCC;CCCCACCTCCACCTGAGCCCGAGAGCTCC)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153296091_153296119del29
CLNSRC
CLNACC	RCV000132912.2,