rs267608639

Orientation

minus

Stabilized

minus

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

Make rs267608639(-;AG)

Make rs267608639(AG;AG)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154030374

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608639
dbSNP (classic)	rs267608639
ClinGen	rs267608639
ebi	rs267608639
HLI	rs267608639
Exac	rs267608639
Gnomad	rs267608639
Varsome	rs267608639
LitVar	rs267608639
Map	rs267608639
PheGenI	rs267608639
Biobank	rs267608639
1000 genomes	rs267608639
hgdp	rs267608639
ensembl	rs267608639
geneview	rs267608639
scholar	rs267608639
google	rs267608639
pharmgkb	rs267608639
gwascentral	rs267608639
openSNP	rs267608639
23andMe	rs267608639
SNPshot	rs267608639
SNPdbe	rs267608639
MSV3d	rs267608639
GWAS Ctlg	rs267608639

Max Magnitude

0

ClinVar
Risk	rs267608639(AG;AG)
Alt	rs267608639(AG;AG)
Reference	Rs267608639(-;-)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153295826_153295827dupCT
CLNSRC
CLNACC	RCV000133015.2,