rs61749709

Orientation

minus

Stabilized

minus

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

Make rs61749709(-;A)

Make rs61749709(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154031260

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs61749709
dbSNP (classic)	rs61749709
ClinGen	rs61749709
ebi	rs61749709
HLI	rs61749709
Exac	rs61749709
Gnomad	rs61749709
Varsome	rs61749709
LitVar	rs61749709
Map	rs61749709
PheGenI	rs61749709
Biobank	rs61749709
1000 genomes	rs61749709
hgdp	rs61749709
ensembl	rs61749709
geneview	rs61749709
scholar	rs61749709
google	rs61749709
pharmgkb	rs61749709
gwascentral	rs61749709
openSNP	rs61749709
23andMe	rs61749709
SNPshot	rs61749709
SNPdbe	rs61749709
MSV3d	rs61749709
GWAS Ctlg	rs61749709

Max Magnitude

0

ClinVar
Risk	rs61749709(A;A)
Alt	rs61749709(A;A)
Reference	Rs61749709(-;-)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153296712dupT
CLNSRC
CLNACC	RCV000133163.2,