rs267608610

Orientation

minus

Stabilized

minus

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

Make rs267608610(-;A)

Make rs267608610(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154030637

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608610
dbSNP (classic)	rs267608610
ClinGen	rs267608610
ebi	rs267608610
HLI	rs267608610
Exac	rs267608610
Gnomad	rs267608610
Varsome	rs267608610
LitVar	rs267608610
Map	rs267608610
PheGenI	rs267608610
Biobank	rs267608610
1000 genomes	rs267608610
hgdp	rs267608610
ensembl	rs267608610
geneview	rs267608610
scholar	rs267608610
google	rs267608610
pharmgkb	rs267608610
gwascentral	rs267608610
openSNP	rs267608610
23andMe	rs267608610
SNPshot	rs267608610
SNPdbe	rs267608610
MSV3d	rs267608610
GWAS Ctlg	rs267608610

Max Magnitude

0

ClinVar
Risk	rs267608610(A;A)
Alt	rs267608610(A;A)
Reference	Rs267608610(-;-)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153296089dupT
CLNSRC
CLNACC	RCV000132954.2,