rs267608409

Orientation

minus

Stabilized

minus

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

Make rs267608409(A;A)

Make rs267608409(A;T)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154092182

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608409
dbSNP (classic)	rs267608409
ClinGen	rs267608409
ebi	rs267608409
HLI	rs267608409
Exac	rs267608409
Gnomad	rs267608409
Varsome	rs267608409
LitVar	rs267608409
Map	rs267608409
PheGenI	rs267608409
Biobank	rs267608409
1000 genomes	rs267608409
hgdp	rs267608409
ensembl	rs267608409
geneview	rs267608409
scholar	rs267608409
google	rs267608409
pharmgkb	rs267608409
gwascentral	rs267608409
openSNP	rs267608409
23andMe	rs267608409
SNPshot	rs267608409
SNPdbe	rs267608409
MSV3d	rs267608409
GWAS Ctlg	rs267608409

Max Magnitude

0

ClinVar
Risk	rs267608409(A;A)
Alt	rs267608409(A;A)
Reference	Rs267608409(T;T)
Significance	Pathogenic
Disease	not provided Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	not provided Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153357640A>T
CLNSRC
CLNACC	RCV000144092.1, RCV000170166.1,