rs61755761

Orientation

minus

Stabilized

minus

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

Make rs61755761(-;-)

Make rs61755761(-;C)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154032239

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs61755761
dbSNP (classic)	rs61755761
ClinGen	rs61755761
ebi	rs61755761
HLI	rs61755761
Exac	rs61755761
Gnomad	rs61755761
Varsome	rs61755761
LitVar	rs61755761
Map	rs61755761
PheGenI	rs61755761
Biobank	rs61755761
1000 genomes	rs61755761
hgdp	rs61755761
ensembl	rs61755761
geneview	rs61755761
scholar	rs61755761
google	rs61755761
pharmgkb	rs61755761
gwascentral	rs61755761
openSNP	rs61755761
23andMe	rs61755761
SNPshot	rs61755761
SNPdbe	rs61755761
MSV3d	rs61755761
GWAS Ctlg	rs61755761

Max Magnitude

0

ClinVar
Risk	rs61755761(-;-)
Alt	rs61755761(-;-)
Reference	Rs61755761(C;C)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153297690delG
CLNSRC
CLNACC	RCV000133075.2,