rs267608444

Orientation

minus

Stabilized

minus

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

Make rs267608444(-;-)

Make rs267608444(-;CA)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154032325

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608444
dbSNP (classic)	rs267608444
ClinGen	rs267608444
ebi	rs267608444
HLI	rs267608444
Exac	rs267608444
Gnomad	rs267608444
Varsome	rs267608444
LitVar	rs267608444
Map	rs267608444
PheGenI	rs267608444
Biobank	rs267608444
1000 genomes	rs267608444
hgdp	rs267608444
ensembl	rs267608444
geneview	rs267608444
scholar	rs267608444
google	rs267608444
pharmgkb	rs267608444
gwascentral	rs267608444
openSNP	rs267608444
23andMe	rs267608444
SNPshot	rs267608444
SNPdbe	rs267608444
MSV3d	rs267608444
GWAS Ctlg	rs267608444

Max Magnitude

0

ClinVar
Risk	rs267608444(-;-)
Alt	rs267608444(-;-)
Reference	Rs267608444(CA;CA)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153297776_153297777delTG
CLNSRC
CLNACC	RCV000133042.2,