rs267608525

Orientation

minus

Stabilized

minus

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

Make rs267608525(C;T)

Make rs267608525(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154031044

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608525
dbSNP (classic)	rs267608525
ClinGen	rs267608525
ebi	rs267608525
HLI	rs267608525
Exac	rs267608525
Gnomad	rs267608525
Varsome	rs267608525
LitVar	rs267608525
Map	rs267608525
PheGenI	rs267608525
Biobank	rs267608525
1000 genomes	rs267608525
hgdp	rs267608525
ensembl	rs267608525
geneview	rs267608525
scholar	rs267608525
google	rs267608525
pharmgkb	rs267608525
gwascentral	rs267608525
openSNP	rs267608525
23andMe	rs267608525
SNPshot	rs267608525
SNPdbe	rs267608525
MSV3d	rs267608525
GWAS Ctlg	rs267608525

Max Magnitude

0

ClinVar
Risk	rs267608525(T;T)
Alt	rs267608525(T;T)
Reference	Rs267608525(C;C)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153296495G>A
CLNSRC	Quest Diagnostics
CLNACC	RCV000133237.3,