rs267608446

Orientation

minus

Stabilized

minus

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

Make rs267608446(-;G)

Make rs267608446(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154032308

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608446
dbSNP (classic)	rs267608446
ClinGen	rs267608446
ebi	rs267608446
HLI	rs267608446
Exac	rs267608446
Gnomad	rs267608446
Varsome	rs267608446
LitVar	rs267608446
Map	rs267608446
PheGenI	rs267608446
Biobank	rs267608446
1000 genomes	rs267608446
hgdp	rs267608446
ensembl	rs267608446
geneview	rs267608446
scholar	rs267608446
google	rs267608446
pharmgkb	rs267608446
gwascentral	rs267608446
openSNP	rs267608446
23andMe	rs267608446
SNPshot	rs267608446
SNPdbe	rs267608446
MSV3d	rs267608446
GWAS Ctlg	rs267608446

Max Magnitude

0

ClinVar
Risk	rs267608446(G;G)
Alt	rs267608446(G;G)
Reference	Rs267608446(-;-)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153297760dupC
CLNSRC
CLNACC	RCV000133044.2,