rs267608417

Orientation

minus

Stabilized

minus

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

Make rs267608417(-;A)

Make rs267608417(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154032527

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608417
dbSNP (classic)	rs267608417
ClinGen	rs267608417
ebi	rs267608417
HLI	rs267608417
Exac	rs267608417
Gnomad	rs267608417
Varsome	rs267608417
LitVar	rs267608417
Map	rs267608417
PheGenI	rs267608417
Biobank	rs267608417
1000 genomes	rs267608417
hgdp	rs267608417
ensembl	rs267608417
geneview	rs267608417
scholar	rs267608417
google	rs267608417
pharmgkb	rs267608417
gwascentral	rs267608417
openSNP	rs267608417
23andMe	rs267608417
SNPshot	rs267608417
SNPdbe	rs267608417
MSV3d	rs267608417
GWAS Ctlg	rs267608417

Max Magnitude

0

ClinVar
Risk	rs267608417(A;A)
Alt	rs267608417(A;A)
Reference	Rs267608417(-;-)
Significance	Pathogenic
Disease	not provided Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	not provided Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153297979dupT
CLNSRC
CLNACC	RCV000133164.2, RCV000194653.1,