rs267608529

Orientation

minus

Stabilized

minus

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

Make rs267608529(-;-)

Make rs267608529(-;AAAG)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154031015

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608529
dbSNP (classic)	rs267608529
ClinGen	rs267608529
ebi	rs267608529
HLI	rs267608529
Exac	rs267608529
Gnomad	rs267608529
Varsome	rs267608529
LitVar	rs267608529
Map	rs267608529
PheGenI	rs267608529
Biobank	rs267608529
1000 genomes	rs267608529
hgdp	rs267608529
ensembl	rs267608529
geneview	rs267608529
scholar	rs267608529
google	rs267608529
pharmgkb	rs267608529
gwascentral	rs267608529
openSNP	rs267608529
23andMe	rs267608529
SNPshot	rs267608529
SNPdbe	rs267608529
MSV3d	rs267608529
GWAS Ctlg	rs267608529

Max Magnitude

0

ClinVar
Risk	rs267608529(-;-)
Alt	rs267608529(-;-)
Reference	Rs267608529(AAAG;AAAG)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153296466_153296469delCTTT
CLNSRC
CLNACC	RCV000133244.2,