rs267608425

Orientation

minus

Stabilized

minus

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

Make rs267608425(-;-)

Make rs267608425(-;AA)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154032476

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608425
dbSNP (classic)	rs267608425
ClinGen	rs267608425
ebi	rs267608425
HLI	rs267608425
Exac	rs267608425
Gnomad	rs267608425
Varsome	rs267608425
LitVar	rs267608425
Map	rs267608425
PheGenI	rs267608425
Biobank	rs267608425
1000 genomes	rs267608425
hgdp	rs267608425
ensembl	rs267608425
geneview	rs267608425
scholar	rs267608425
google	rs267608425
pharmgkb	rs267608425
gwascentral	rs267608425
openSNP	rs267608425
23andMe	rs267608425
SNPshot	rs267608425
SNPdbe	rs267608425
MSV3d	rs267608425
GWAS Ctlg	rs267608425

Max Magnitude

0

ClinVar
Risk	rs267608425(-;-)
Alt	rs267608425(-;-)
Reference	Rs267608425(AA;AA)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153297927_153297928delTT
CLNSRC
CLNACC	RCV000132848.2,