rs267608634

Orientation

minus

Stabilized

minus

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

Make rs267608634(-;-)

Make rs267608634(-;AG)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154030412

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608634
dbSNP (classic)	rs267608634
ClinGen	rs267608634
ebi	rs267608634
HLI	rs267608634
Exac	rs267608634
Gnomad	rs267608634
Varsome	rs267608634
LitVar	rs267608634
Map	rs267608634
PheGenI	rs267608634
Biobank	rs267608634
1000 genomes	rs267608634
hgdp	rs267608634
ensembl	rs267608634
geneview	rs267608634
scholar	rs267608634
google	rs267608634
pharmgkb	rs267608634
gwascentral	rs267608634
openSNP	rs267608634
23andMe	rs267608634
SNPshot	rs267608634
SNPdbe	rs267608634
MSV3d	rs267608634
GWAS Ctlg	rs267608634

Max Magnitude

0

ClinVar
Risk	rs267608634(-;-)
Alt	rs267608634(-;-)
Reference	Rs267608634(AG;AG)
Significance	Pathogenic
Disease	Mental retardation
Variation	info
Gene	MECP2
CLNDBN	Mental retardation, X-linked, syndromic 13
Reversed	1
HGVS	NC_000023.10:g.153295863_153295864delCT
CLNSRC
CLNACC	RCV000133004.2,