rs61749727

Orientation

minus

Stabilized

minus

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

Make rs61749727(-;-)

Make rs61749727(-;G)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154031211

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs61749727
dbSNP (classic)	rs61749727
ClinGen	rs61749727
ebi	rs61749727
HLI	rs61749727
Exac	rs61749727
Gnomad	rs61749727
Varsome	rs61749727
LitVar	rs61749727
Map	rs61749727
PheGenI	rs61749727
Biobank	rs61749727
1000 genomes	rs61749727
hgdp	rs61749727
ensembl	rs61749727
geneview	rs61749727
scholar	rs61749727
google	rs61749727
pharmgkb	rs61749727
gwascentral	rs61749727
openSNP	rs61749727
23andMe	rs61749727
SNPshot	rs61749727
SNPdbe	rs61749727
MSV3d	rs61749727
GWAS Ctlg	rs61749727

Max Magnitude

0

ClinVar
Risk	rs61749727(-;-)
Alt	rs61749727(-;-)
Reference	Rs61749727(G;G)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153296662delC
CLNSRC
CLNACC	RCV000133179.2,