rs267608487

Orientation

minus

Stabilized

minus

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

Make rs267608487(-;A)

Make rs267608487(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154031343

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608487
dbSNP (classic)	rs267608487
ClinGen	rs267608487
ebi	rs267608487
HLI	rs267608487
Exac	rs267608487
Gnomad	rs267608487
Varsome	rs267608487
LitVar	rs267608487
Map	rs267608487
PheGenI	rs267608487
Biobank	rs267608487
1000 genomes	rs267608487
hgdp	rs267608487
ensembl	rs267608487
geneview	rs267608487
scholar	rs267608487
google	rs267608487
pharmgkb	rs267608487
gwascentral	rs267608487
openSNP	rs267608487
23andMe	rs267608487
SNPshot	rs267608487
SNPdbe	rs267608487
MSV3d	rs267608487
GWAS Ctlg	rs267608487

Max Magnitude

0

ClinVar
Risk	rs267608487(A;A)
Alt	rs267608487(A;A)
Reference	Rs267608487(-;-)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153296795dupT
CLNSRC
CLNACC	RCV000133139.2,