rs267608455

Orientation

minus

Stabilized

minus

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

Make rs267608455(A;A)

Make rs267608455(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

X

Position

154032220

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608455
dbSNP (classic)	rs267608455
ClinGen	rs267608455
ebi	rs267608455
HLI	rs267608455
Exac	rs267608455
Gnomad	rs267608455
Varsome	rs267608455
LitVar	rs267608455
Map	rs267608455
PheGenI	rs267608455
Biobank	rs267608455
1000 genomes	rs267608455
hgdp	rs267608455
ensembl	rs267608455
geneview	rs267608455
scholar	rs267608455
google	rs267608455
pharmgkb	rs267608455
gwascentral	rs267608455
openSNP	rs267608455
23andMe	rs267608455
SNPshot	rs267608455
SNPdbe	rs267608455
MSV3d	rs267608455
GWAS Ctlg	rs267608455

Max Magnitude

0

ClinVar
Risk	rs267608455(A;A)
Alt	rs267608455(A;A)
Reference	Rs267608455(G;G)
Significance	Pathogenic
Disease	Rett syndrome not provided
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome not provided
Reversed	1
HGVS	NC_000023.10:g.153297671C>T
CLNSRC
CLNACC	RCV000133079.2, RCV000254852.1,