rs267608624

Orientation

minus

Stabilized

minus

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

Make rs267608624(-;T)

Make rs267608624(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154030507

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608624
dbSNP (classic)	rs267608624
ClinGen	rs267608624
ebi	rs267608624
HLI	rs267608624
Exac	rs267608624
Gnomad	rs267608624
Varsome	rs267608624
LitVar	rs267608624
Map	rs267608624
PheGenI	rs267608624
Biobank	rs267608624
1000 genomes	rs267608624
hgdp	rs267608624
ensembl	rs267608624
geneview	rs267608624
scholar	rs267608624
google	rs267608624
pharmgkb	rs267608624
gwascentral	rs267608624
openSNP	rs267608624
23andMe	rs267608624
SNPshot	rs267608624
SNPdbe	rs267608624
MSV3d	rs267608624
GWAS Ctlg	rs267608624

Max Magnitude

0

ClinVar
Risk	rs267608624(T;T)
Alt	rs267608624(T;T)
Reference	Rs267608624(-;-)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153295959dupA
CLNSRC
CLNACC	RCV000132987.2,