rs267608343

Orientation

minus

Stabilized

minus

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

Make rs267608343(-;-)

Make rs267608343(-;TCCACCTGAGCCCGAGAGCTCCGAGGACCCCACC)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154030628

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608343
dbSNP (classic)	rs267608343
ClinGen	rs267608343
ebi	rs267608343
HLI	rs267608343
Exac	rs267608343
Gnomad	rs267608343
Varsome	rs267608343
LitVar	rs267608343
Map	rs267608343
PheGenI	rs267608343
Biobank	rs267608343
1000 genomes	rs267608343
hgdp	rs267608343
ensembl	rs267608343
geneview	rs267608343
scholar	rs267608343
google	rs267608343
pharmgkb	rs267608343
gwascentral	rs267608343
openSNP	rs267608343
23andMe	rs267608343
SNPshot	rs267608343
SNPdbe	rs267608343
MSV3d	rs267608343
GWAS Ctlg	rs267608343

Max Magnitude

0

ClinVar
Risk	rs267608343(-;-)
Alt	rs267608343(-;-)
Reference	Rs267608343(TCCACCTGAGCCCGAGAGCTCCGAGGACCCCACC;TCCACCTGAGCCCGAGAGCTCCGAGGACCCCACC)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153296079_153296112del34
CLNSRC
CLNACC	RCV000132937.2,