rs786205020

Orientation

minus

Stabilized

minus

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

Make rs786205020(-;-)

Make rs786205020(-;ACCTCCACCTGAGCCCGAGAGCTCCGAGGAC)

Reference

GRCh38.p2 38.2/146

Chromosome

X

Position

154030634

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs786205020
dbSNP (classic)	rs786205020
ClinGen	rs786205020
ebi	rs786205020
HLI	rs786205020
Exac	rs786205020
Gnomad	rs786205020
Varsome	rs786205020
LitVar	rs786205020
Map	rs786205020
PheGenI	rs786205020
Biobank	rs786205020
1000 genomes	rs786205020
hgdp	rs786205020
ensembl	rs786205020
geneview	rs786205020
scholar	rs786205020
google	rs786205020
pharmgkb	rs786205020
gwascentral	rs786205020
openSNP	rs786205020
23andMe	rs786205020
SNPshot	rs786205020
SNPdbe	rs786205020
MSV3d	rs786205020
GWAS Ctlg	rs786205020

Max Magnitude

0

ClinVar
Risk	rs786205020(-;-)
Alt	rs786205020(-;-)
Reference	Rs786205020(ACCTCCACCTGAGCCCGAGAGCTCCGAGGAC;ACCTCCACCTGAGCCCGAGAGCTCCGAGGAC)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153296085_153296115del31
CLNSRC
CLNACC	RCV000170151.1,