rs267608416

Orientation

minus

Stabilized

minus

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

Make rs267608416(-;A)

Make rs267608416(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154032533

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608416
dbSNP (classic)	rs267608416
ClinGen	rs267608416
ebi	rs267608416
HLI	rs267608416
Exac	rs267608416
Gnomad	rs267608416
Varsome	rs267608416
LitVar	rs267608416
Map	rs267608416
PheGenI	rs267608416
Biobank	rs267608416
1000 genomes	rs267608416
hgdp	rs267608416
ensembl	rs267608416
geneview	rs267608416
scholar	rs267608416
google	rs267608416
pharmgkb	rs267608416
gwascentral	rs267608416
openSNP	rs267608416
23andMe	rs267608416
SNPshot	rs267608416
SNPdbe	rs267608416
MSV3d	rs267608416
GWAS Ctlg	rs267608416

Max Magnitude

0

ClinVar
Risk	rs267608416(A;A)
Alt	rs267608416(A;A)
Reference	Rs267608416(-;-)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153297985dupT
CLNSRC
CLNACC	RCV000133145.2,