rs267608329

Orientation

minus

Stabilized

minus

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

Make rs267608329(-;-)

Make rs267608329(-;CCTGCCCCCACCTCCACCTGAGCCCGAGAGCTCCGAGGACCCCACC)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154030628

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608329
dbSNP (classic)	rs267608329
ClinGen	rs267608329
ebi	rs267608329
HLI	rs267608329
Exac	rs267608329
Gnomad	rs267608329
Varsome	rs267608329
LitVar	rs267608329
Map	rs267608329
PheGenI	rs267608329
Biobank	rs267608329
1000 genomes	rs267608329
hgdp	rs267608329
ensembl	rs267608329
geneview	rs267608329
scholar	rs267608329
google	rs267608329
pharmgkb	rs267608329
gwascentral	rs267608329
openSNP	rs267608329
23andMe	rs267608329
SNPshot	rs267608329
SNPdbe	rs267608329
MSV3d	rs267608329
GWAS Ctlg	rs267608329

Max Magnitude

0

ClinVar
Risk	rs267608329(-;-)
Alt	rs267608329(-;-)
Reference	Rs267608329(CCTGCCCCCACCTCCACCTGAGCCCGAGAGCTCCGAGGACCCCACC;CCTGCCCCCACCTCCACCTGAGCCCGAGAGCTCCGAGGACCCCACC)
Significance	Pathogenic
Disease	Rett syndrome not provided
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome not provided
Reversed	1
HGVS	NC_000023.10:g.153296079_153296124del46
CLNSRC
CLNACC	RCV000132886.2, RCV000479970.1,