rs61749708

Orientation

minus

Stabilized

minus

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

Make rs61749708(-;-)

Make rs61749708(-;G)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154031262

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs61749708
dbSNP (classic)	rs61749708
ClinGen	rs61749708
ebi	rs61749708
HLI	rs61749708
Exac	rs61749708
Gnomad	rs61749708
Varsome	rs61749708
LitVar	rs61749708
Map	rs61749708
PheGenI	rs61749708
Biobank	rs61749708
1000 genomes	rs61749708
hgdp	rs61749708
ensembl	rs61749708
geneview	rs61749708
scholar	rs61749708
google	rs61749708
pharmgkb	rs61749708
gwascentral	rs61749708
openSNP	rs61749708
23andMe	rs61749708
SNPshot	rs61749708
SNPdbe	rs61749708
MSV3d	rs61749708
GWAS Ctlg	rs61749708

Max Magnitude

0

ClinVar
Risk	rs61749708(-;-)
Alt	rs61749708(-;-)
Reference	Rs61749708(G;G)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153296713delC
CLNSRC
CLNACC	RCV000133161.2,