rs267608449

Orientation

minus

Stabilized

minus

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

Make rs267608449(-;-)

Make rs267608449(-;ACC)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154032287

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608449
dbSNP (classic)	rs267608449
ClinGen	rs267608449
ebi	rs267608449
HLI	rs267608449
Exac	rs267608449
Gnomad	rs267608449
Varsome	rs267608449
LitVar	rs267608449
Map	rs267608449
PheGenI	rs267608449
Biobank	rs267608449
1000 genomes	rs267608449
hgdp	rs267608449
ensembl	rs267608449
geneview	rs267608449
scholar	rs267608449
google	rs267608449
pharmgkb	rs267608449
gwascentral	rs267608449
openSNP	rs267608449
23andMe	rs267608449
SNPshot	rs267608449
SNPdbe	rs267608449
MSV3d	rs267608449
GWAS Ctlg	rs267608449

Max Magnitude

0

ClinVar
Risk	rs267608449(-;-)
Alt	rs267608449(-;-)
Reference	Rs267608449(ACC;ACC)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153297738_153297740delGGT
CLNSRC
CLNACC	RCV000133052.2,