rs267608482

Orientation

minus

Stabilized

minus

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

Make rs267608482(-;T)

Make rs267608482(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154031357

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608482
dbSNP (classic)	rs267608482
ClinGen	rs267608482
ebi	rs267608482
HLI	rs267608482
Exac	rs267608482
Gnomad	rs267608482
Varsome	rs267608482
LitVar	rs267608482
Map	rs267608482
PheGenI	rs267608482
Biobank	rs267608482
1000 genomes	rs267608482
hgdp	rs267608482
ensembl	rs267608482
geneview	rs267608482
scholar	rs267608482
google	rs267608482
pharmgkb	rs267608482
gwascentral	rs267608482
openSNP	rs267608482
23andMe	rs267608482
SNPshot	rs267608482
SNPdbe	rs267608482
MSV3d	rs267608482
GWAS Ctlg	rs267608482

Max Magnitude

0

ClinVar
Risk	rs267608482(T;T)
Alt	rs267608482(T;T)
Reference	Rs267608482(-;-)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153296809dupA
CLNSRC
CLNACC	RCV000133126.2,