rs267608548

Orientation

minus

Stabilized

minus

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

Make rs267608548(-;-)

Make rs267608548(-;C)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154030922

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608548
dbSNP (classic)	rs267608548
ClinGen	rs267608548
ebi	rs267608548
HLI	rs267608548
Exac	rs267608548
Gnomad	rs267608548
Varsome	rs267608548
LitVar	rs267608548
Map	rs267608548
PheGenI	rs267608548
Biobank	rs267608548
1000 genomes	rs267608548
hgdp	rs267608548
ensembl	rs267608548
geneview	rs267608548
scholar	rs267608548
google	rs267608548
pharmgkb	rs267608548
gwascentral	rs267608548
openSNP	rs267608548
23andMe	rs267608548
SNPshot	rs267608548
SNPdbe	rs267608548
MSV3d	rs267608548
GWAS Ctlg	rs267608548

Max Magnitude

0

ClinVar
Risk	rs267608548(-;-)
Alt	rs267608548(-;-)
Reference	Rs267608548(C;C)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153296373delG
CLNSRC
CLNACC	RCV000133283.2,