rs267608606

Orientation

minus

Stabilized

minus

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

Make rs267608606(-;-)

Make rs267608606(-;A)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154030664

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608606
dbSNP (classic)	rs267608606
ClinGen	rs267608606
ebi	rs267608606
HLI	rs267608606
Exac	rs267608606
Gnomad	rs267608606
Varsome	rs267608606
LitVar	rs267608606
Map	rs267608606
PheGenI	rs267608606
Biobank	rs267608606
1000 genomes	rs267608606
hgdp	rs267608606
ensembl	rs267608606
geneview	rs267608606
scholar	rs267608606
google	rs267608606
pharmgkb	rs267608606
gwascentral	rs267608606
openSNP	rs267608606
23andMe	rs267608606
SNPshot	rs267608606
SNPdbe	rs267608606
MSV3d	rs267608606
GWAS Ctlg	rs267608606

Max Magnitude

0

ClinVar
Risk	rs267608606(-;-)
Alt	rs267608606(-;-)
Reference	Rs267608606(A;A)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153296115delT
CLNSRC
CLNACC	RCV000132934.2,