rs267608427

Orientation

minus

Stabilized

minus

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

Make rs267608427(-;A)

Make rs267608427(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154032466

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608427
dbSNP (classic)	rs267608427
ClinGen	rs267608427
ebi	rs267608427
HLI	rs267608427
Exac	rs267608427
Gnomad	rs267608427
Varsome	rs267608427
LitVar	rs267608427
Map	rs267608427
PheGenI	rs267608427
Biobank	rs267608427
1000 genomes	rs267608427
hgdp	rs267608427
ensembl	rs267608427
geneview	rs267608427
scholar	rs267608427
google	rs267608427
pharmgkb	rs267608427
gwascentral	rs267608427
openSNP	rs267608427
23andMe	rs267608427
SNPshot	rs267608427
SNPdbe	rs267608427
MSV3d	rs267608427
GWAS Ctlg	rs267608427

Max Magnitude

0

ClinVar
Risk	rs267608427(A;A)
Alt	rs267608427(A;A)
Reference	Rs267608427(-;-)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153297918dupT
CLNSRC
CLNACC	RCV000132946.2,