rs267608510

Orientation

minus

Stabilized

minus

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

Make rs267608510(-;-)

Make rs267608510(-;TG)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154031176

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608510
dbSNP (classic)	rs267608510
ClinGen	rs267608510
ebi	rs267608510
HLI	rs267608510
Exac	rs267608510
Gnomad	rs267608510
Varsome	rs267608510
LitVar	rs267608510
Map	rs267608510
PheGenI	rs267608510
Biobank	rs267608510
1000 genomes	rs267608510
hgdp	rs267608510
ensembl	rs267608510
geneview	rs267608510
scholar	rs267608510
google	rs267608510
pharmgkb	rs267608510
gwascentral	rs267608510
openSNP	rs267608510
23andMe	rs267608510
SNPshot	rs267608510
SNPdbe	rs267608510
MSV3d	rs267608510
GWAS Ctlg	rs267608510

Max Magnitude

0

ClinVar
Risk	rs267608510(-;-)
Alt	rs267608510(-;-)
Reference	Rs267608510(TG;TG)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153296627_153296628delCA
CLNSRC
CLNACC	RCV000133188.2,