rs267608424

Orientation

minus

Stabilized

minus

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

Make rs267608424(-;-)

Make rs267608424(-;AAGAAGA)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154032471

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608424
dbSNP (classic)	rs267608424
ClinGen	rs267608424
ebi	rs267608424
HLI	rs267608424
Exac	rs267608424
Gnomad	rs267608424
Varsome	rs267608424
LitVar	rs267608424
Map	rs267608424
PheGenI	rs267608424
Biobank	rs267608424
1000 genomes	rs267608424
hgdp	rs267608424
ensembl	rs267608424
geneview	rs267608424
scholar	rs267608424
google	rs267608424
pharmgkb	rs267608424
gwascentral	rs267608424
openSNP	rs267608424
23andMe	rs267608424
SNPshot	rs267608424
SNPdbe	rs267608424
MSV3d	rs267608424
GWAS Ctlg	rs267608424

Max Magnitude

0

ClinVar
Risk	rs267608424(-;-)
Alt	rs267608424(-;-)
Reference	Rs267608424(AAGAAGA;AAGAAGA)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153297922_153297928delTCTTCTT
CLNSRC
CLNACC	RCV000132849.2,