rs267608503

Orientation

minus

Stabilized

minus

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

Make rs267608503(-;G)

Make rs267608503(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154031226

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608503
dbSNP (classic)	rs267608503
ClinGen	rs267608503
ebi	rs267608503
HLI	rs267608503
Exac	rs267608503
Gnomad	rs267608503
Varsome	rs267608503
LitVar	rs267608503
Map	rs267608503
PheGenI	rs267608503
Biobank	rs267608503
1000 genomes	rs267608503
hgdp	rs267608503
ensembl	rs267608503
geneview	rs267608503
scholar	rs267608503
google	rs267608503
pharmgkb	rs267608503
gwascentral	rs267608503
openSNP	rs267608503
23andMe	rs267608503
SNPshot	rs267608503
SNPdbe	rs267608503
MSV3d	rs267608503
GWAS Ctlg	rs267608503

Max Magnitude

0

ClinVar
Risk	rs267608503(G;G)
Alt	rs267608503(G;G)
Reference	Rs267608503(-;-)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153296678dupC
CLNSRC
CLNACC	RCV000133172.2,