rs267608386

Orientation

minus

Stabilized

minus

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

Make rs267608386(-;-)

Make rs267608386(-;AGAAAAGTCCTGG)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154031175

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608386
dbSNP (classic)	rs267608386
ClinGen	rs267608386
ebi	rs267608386
HLI	rs267608386
Exac	rs267608386
Gnomad	rs267608386
Varsome	rs267608386
LitVar	rs267608386
Map	rs267608386
PheGenI	rs267608386
Biobank	rs267608386
1000 genomes	rs267608386
hgdp	rs267608386
ensembl	rs267608386
geneview	rs267608386
scholar	rs267608386
google	rs267608386
pharmgkb	rs267608386
gwascentral	rs267608386
openSNP	rs267608386
23andMe	rs267608386
SNPshot	rs267608386
SNPdbe	rs267608386
MSV3d	rs267608386
GWAS Ctlg	rs267608386

Max Magnitude

0

ClinVar
Risk	rs267608386(-;-)
Alt	rs267608386(-;-)
Reference	Rs267608386(AGAAAAGTCCTGG;AGAAAAGTCCTGG)
Significance	Probable-Pathogenic
Disease	not provided Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	not provided Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153296626_153296638delCCAGGACTTTTCT
CLNSRC	Children's Hospital of Eastern Ontario
CLNACC	RCV000133186.1, RCV000168686.2,