rs267608492

Orientation

minus

Stabilized

minus

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

Make rs267608492(C;G)

Make rs267608492(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

154031310

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608492
dbSNP (classic)	rs267608492
ClinGen	rs267608492
ebi	rs267608492
HLI	rs267608492
Exac	rs267608492
Gnomad	rs267608492
Varsome	rs267608492
LitVar	rs267608492
Map	rs267608492
PheGenI	rs267608492
Biobank	rs267608492
1000 genomes	rs267608492
hgdp	rs267608492
ensembl	rs267608492
geneview	rs267608492
scholar	rs267608492
google	rs267608492
pharmgkb	rs267608492
gwascentral	rs267608492
openSNP	rs267608492
23andMe	rs267608492
SNPshot	rs267608492
SNPdbe	rs267608492
MSV3d	rs267608492
GWAS Ctlg	rs267608492

Max Magnitude

0

ClinVar
Risk	rs267608492(G;G)
Alt	rs267608492(G;G)
Reference	Rs267608492(C;C)
Significance	Other
Disease	not specified Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	not specified Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153296761G>C
CLNSRC
CLNACC	RCV000133149.2, RCV000192592.1,