rs267608445

Orientation

minus

Stabilized

minus

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

Make rs267608445(G;T)

Make rs267608445(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154032310

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608445
dbSNP (classic)	rs267608445
ClinGen	rs267608445
ebi	rs267608445
HLI	rs267608445
Exac	rs267608445
Gnomad	rs267608445
Varsome	rs267608445
LitVar	rs267608445
Map	rs267608445
PheGenI	rs267608445
Biobank	rs267608445
1000 genomes	rs267608445
hgdp	rs267608445
ensembl	rs267608445
geneview	rs267608445
scholar	rs267608445
google	rs267608445
pharmgkb	rs267608445
gwascentral	rs267608445
openSNP	rs267608445
23andMe	rs267608445
SNPshot	rs267608445
SNPdbe	rs267608445
MSV3d	rs267608445
GWAS Ctlg	rs267608445

Max Magnitude

0

ClinVar
Risk	rs267608445(T;T)
Alt	rs267608445(T;T)
Reference	Rs267608445(G;G)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153297761C>A
CLNSRC
CLNACC	RCV000133043.2,