rs267608388

Orientation

minus

Stabilized

minus

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

Make rs267608388(C;T)

Make rs267608388(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

154032241

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608388
dbSNP (classic)	rs267608388
ClinGen	rs267608388
ebi	rs267608388
HLI	rs267608388
Exac	rs267608388
Gnomad	rs267608388
Varsome	rs267608388
LitVar	rs267608388
Map	rs267608388
PheGenI	rs267608388
Biobank	rs267608388
1000 genomes	rs267608388
hgdp	rs267608388
ensembl	rs267608388
geneview	rs267608388
scholar	rs267608388
google	rs267608388
pharmgkb	rs267608388
gwascentral	rs267608388
openSNP	rs267608388
23andMe	rs267608388
SNPshot	rs267608388
SNPdbe	rs267608388
MSV3d	rs267608388
GWAS Ctlg	rs267608388

Max Magnitude

0

ClinVar
Risk	rs267608388(T;T)
Alt	rs267608388(T;T)
Reference	Rs267608388(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MECP2
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.153297692G>A
CLNSRC
CLNACC	RCV000133074.4,