rs267608576

Orientation

minus

Stabilized

minus

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

Make rs267608576(-;-)

Make rs267608576(-;ACCC)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154030673

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608576
dbSNP (classic)	rs267608576
ClinGen	rs267608576
ebi	rs267608576
HLI	rs267608576
Exac	rs267608576
Gnomad	rs267608576
Varsome	rs267608576
LitVar	rs267608576
Map	rs267608576
PheGenI	rs267608576
Biobank	rs267608576
1000 genomes	rs267608576
hgdp	rs267608576
ensembl	rs267608576
geneview	rs267608576
scholar	rs267608576
google	rs267608576
pharmgkb	rs267608576
gwascentral	rs267608576
openSNP	rs267608576
23andMe	rs267608576
SNPshot	rs267608576
SNPdbe	rs267608576
MSV3d	rs267608576
GWAS Ctlg	rs267608576

Max Magnitude

0

ClinVar
Risk	rs267608576(-;-)
Alt	rs267608576(-;-)
Reference	Rs267608576(ACCC;ACCC)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153296124_153296127delGGGT
CLNSRC
CLNACC	RCV000132879.2,