rs267608567

Orientation

minus

Stabilized

minus

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

Make rs267608567(-;-)

Make rs267608567(-;CACCACCATCACCACCACTC)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154030710

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608567
dbSNP (classic)	rs267608567
ClinGen	rs267608567
ebi	rs267608567
HLI	rs267608567
Exac	rs267608567
Gnomad	rs267608567
Varsome	rs267608567
LitVar	rs267608567
Map	rs267608567
PheGenI	rs267608567
Biobank	rs267608567
1000 genomes	rs267608567
hgdp	rs267608567
ensembl	rs267608567
geneview	rs267608567
scholar	rs267608567
google	rs267608567
pharmgkb	rs267608567
gwascentral	rs267608567
openSNP	rs267608567
23andMe	rs267608567
SNPshot	rs267608567
SNPdbe	rs267608567
MSV3d	rs267608567
GWAS Ctlg	rs267608567

Max Magnitude

0

ClinVar
Risk	rs267608567(-;-)
Alt	rs267608567(-;-)
Reference	Rs267608567(CACCACCATCACCACCACTC;CACCACCATCACCACCACTC)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153296161_153296180del20
CLNSRC
CLNACC	RCV000132854.2,