rs61753011

Orientation

minus

Stabilized

minus

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

Make rs61753011(-;T)

Make rs61753011(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154030633

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs61753011
dbSNP (classic)	rs61753011
ClinGen	rs61753011
ebi	rs61753011
HLI	rs61753011
Exac	rs61753011
Gnomad	rs61753011
Varsome	rs61753011
LitVar	rs61753011
Map	rs61753011
PheGenI	rs61753011
Biobank	rs61753011
1000 genomes	rs61753011
hgdp	rs61753011
ensembl	rs61753011
geneview	rs61753011
scholar	rs61753011
google	rs61753011
pharmgkb	rs61753011
gwascentral	rs61753011
openSNP	rs61753011
23andMe	rs61753011
SNPshot	rs61753011
SNPdbe	rs61753011
MSV3d	rs61753011
GWAS Ctlg	rs61753011

Max Magnitude

0

ClinVar
Risk	rs61753011(T;T)
Alt	rs61753011(T;T)
Reference	Rs61753011(-;-)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153296084_153296085insA
CLNSRC
CLNACC	RCV000132955.2,