rs267608442

Orientation

minus

Stabilized

minus

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

Make rs267608442(-;-)

Make rs267608442(-;C)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154032351

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608442
dbSNP (classic)	rs267608442
ClinGen	rs267608442
ebi	rs267608442
HLI	rs267608442
Exac	rs267608442
Gnomad	rs267608442
Varsome	rs267608442
LitVar	rs267608442
Map	rs267608442
PheGenI	rs267608442
Biobank	rs267608442
1000 genomes	rs267608442
hgdp	rs267608442
ensembl	rs267608442
geneview	rs267608442
scholar	rs267608442
google	rs267608442
pharmgkb	rs267608442
gwascentral	rs267608442
openSNP	rs267608442
23andMe	rs267608442
SNPshot	rs267608442
SNPdbe	rs267608442
MSV3d	rs267608442
GWAS Ctlg	rs267608442

Max Magnitude

0

ClinVar
Risk	rs267608442(-;-)
Alt	rs267608442(-;-)
Reference	Rs267608442(C;C)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153297802delG
CLNSRC
CLNACC	RCV000133038.2,