rs267608438

Orientation

minus

Stabilized

minus

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

Make rs267608438(C;G)

Make rs267608438(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154032381

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608438
dbSNP (classic)	rs267608438
ClinGen	rs267608438
ebi	rs267608438
HLI	rs267608438
Exac	rs267608438
Gnomad	rs267608438
Varsome	rs267608438
LitVar	rs267608438
Map	rs267608438
PheGenI	rs267608438
Biobank	rs267608438
1000 genomes	rs267608438
hgdp	rs267608438
ensembl	rs267608438
geneview	rs267608438
scholar	rs267608438
google	rs267608438
pharmgkb	rs267608438
gwascentral	rs267608438
openSNP	rs267608438
23andMe	rs267608438
SNPshot	rs267608438
SNPdbe	rs267608438
MSV3d	rs267608438
GWAS Ctlg	rs267608438

Max Magnitude

0

ClinVar
Risk	rs267608438(G;G)
Alt	rs267608438(G;G)
Reference	Rs267608438(C;C)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153297832G>C
CLNSRC
CLNACC	RCV000133031.2,