rs786205025

Orientation

minus

Stabilized

minus

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

Make rs786205025(-;GAAG)

Make rs786205025(GAAG;GAAG)

Reference

GRCh38.p2 38.2/146

Chromosome

X

Position

154032262

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs786205025
dbSNP (classic)	rs786205025
ClinGen	rs786205025
ebi	rs786205025
HLI	rs786205025
Exac	rs786205025
Gnomad	rs786205025
Varsome	rs786205025
LitVar	rs786205025
Map	rs786205025
PheGenI	rs786205025
Biobank	rs786205025
1000 genomes	rs786205025
hgdp	rs786205025
ensembl	rs786205025
geneview	rs786205025
scholar	rs786205025
google	rs786205025
pharmgkb	rs786205025
gwascentral	rs786205025
openSNP	rs786205025
23andMe	rs786205025
SNPshot	rs786205025
SNPdbe	rs786205025
MSV3d	rs786205025
GWAS Ctlg	rs786205025

Max Magnitude

0

ClinVar
Risk	rs786205025(GAAG;GAAG)
Alt	rs786205025(GAAG;GAAG)
Reference	Rs786205025(-;-)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153297714_153297717dupCTTC
CLNSRC
CLNACC	RCV000170189.1,