rs267608452

Orientation

minus

Stabilized

minus

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

Make rs267608452(-;A)

Make rs267608452(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154032257

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608452
dbSNP (classic)	rs267608452
ClinGen	rs267608452
ebi	rs267608452
HLI	rs267608452
Exac	rs267608452
Gnomad	rs267608452
Varsome	rs267608452
LitVar	rs267608452
Map	rs267608452
PheGenI	rs267608452
Biobank	rs267608452
1000 genomes	rs267608452
hgdp	rs267608452
ensembl	rs267608452
geneview	rs267608452
scholar	rs267608452
google	rs267608452
pharmgkb	rs267608452
gwascentral	rs267608452
openSNP	rs267608452
23andMe	rs267608452
SNPshot	rs267608452
SNPdbe	rs267608452
MSV3d	rs267608452
GWAS Ctlg	rs267608452

Max Magnitude

0

ClinVar
Risk	rs267608452(A;A)
Alt	rs267608452(A;A)
Reference	Rs267608452(-;-)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153297709dupT
CLNSRC
CLNACC	RCV000133070.2,