rs267608411

Orientation

minus

Stabilized

minus

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

Make rs267608411(C;G)

Make rs267608411(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154032563

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608411
dbSNP (classic)	rs267608411
ClinGen	rs267608411
ebi	rs267608411
HLI	rs267608411
Exac	rs267608411
Gnomad	rs267608411
Varsome	rs267608411
LitVar	rs267608411
Map	rs267608411
PheGenI	rs267608411
Biobank	rs267608411
1000 genomes	rs267608411
hgdp	rs267608411
ensembl	rs267608411
geneview	rs267608411
scholar	rs267608411
google	rs267608411
pharmgkb	rs267608411
gwascentral	rs267608411
openSNP	rs267608411
23andMe	rs267608411
SNPshot	rs267608411
SNPdbe	rs267608411
MSV3d	rs267608411
GWAS Ctlg	rs267608411

Max Magnitude

0

ClinVar
Risk	rs267608411(G;G)
Alt	rs267608411(G;G)
Reference	Rs267608411(C;C)
Significance	Pathogenic
Disease	not provided Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	not provided Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153298014G>C
CLNSRC
CLNACC	RCV000144095.1, RCV000170187.2,