rs267608465

Orientation

minus

Stabilized

minus

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

Make rs267608465(C;G)

Make rs267608465(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154031453

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608465
dbSNP (classic)	rs267608465
ClinGen	rs267608465
ebi	rs267608465
HLI	rs267608465
Exac	rs267608465
Gnomad	rs267608465
Varsome	rs267608465
LitVar	rs267608465
Map	rs267608465
PheGenI	rs267608465
Biobank	rs267608465
1000 genomes	rs267608465
hgdp	rs267608465
ensembl	rs267608465
geneview	rs267608465
scholar	rs267608465
google	rs267608465
pharmgkb	rs267608465
gwascentral	rs267608465
openSNP	rs267608465
23andMe	rs267608465
SNPshot	rs267608465
SNPdbe	rs267608465
MSV3d	rs267608465
GWAS Ctlg	rs267608465

Max Magnitude

0

ClinVar
Risk	rs267608465(G;G) rs267608465(T;T)
Alt	rs267608465(G;G) rs267608465(T;T)
Reference	Rs267608465(C;C)
Significance	Pathogenic
Disease	not provided Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	not provided Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153296904G>C
CLNSRC
CLNACC	RCV000144115.2, RCV000170202.1,