rs267608333

Orientation

minus

Stabilized

minus

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

Make rs267608333(-;-)

Make rs267608333(-;GAGAGCTCCGAGGACCCCACCAGCCC)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

154030623

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608333
dbSNP (classic)	rs267608333
ClinGen	rs267608333
ebi	rs267608333
HLI	rs267608333
Exac	rs267608333
Gnomad	rs267608333
Varsome	rs267608333
LitVar	rs267608333
Map	rs267608333
PheGenI	rs267608333
Biobank	rs267608333
1000 genomes	rs267608333
hgdp	rs267608333
ensembl	rs267608333
geneview	rs267608333
scholar	rs267608333
google	rs267608333
pharmgkb	rs267608333
gwascentral	rs267608333
openSNP	rs267608333
23andMe	rs267608333
SNPshot	rs267608333
SNPdbe	rs267608333
MSV3d	rs267608333
GWAS Ctlg	rs267608333

Max Magnitude

0

ClinVar
Risk	rs267608333(-;-)
Alt	rs267608333(-;-)
Reference	Rs267608333(GAGAGCTCCGAGGACCCCACCAGCCC;GAGAGCTCCGAGGACCCCACCAGCCC)
Significance	Pathogenic
Disease	not provided Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	not provided Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153296074_153296099del26
CLNSRC
CLNACC	RCV000132948.1, RCV000445571.1,