rs786205892

Orientation

minus

Stabilized

minus

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

Make rs786205892(A;T)

Make rs786205892(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

X

Position

154092209

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs786205892
dbSNP (classic)	rs786205892
ClinGen	rs786205892
ebi	rs786205892
HLI	rs786205892
Exac	rs786205892
Gnomad	rs786205892
Varsome	rs786205892
LitVar	rs786205892
Map	rs786205892
PheGenI	rs786205892
Biobank	rs786205892
1000 genomes	rs786205892
hgdp	rs786205892
ensembl	rs786205892
geneview	rs786205892
scholar	rs786205892
google	rs786205892
pharmgkb	rs786205892
gwascentral	rs786205892
openSNP	rs786205892
23andMe	rs786205892
SNPshot	rs786205892
SNPdbe	rs786205892
MSV3d	rs786205892
GWAS Ctlg	rs786205892

Max Magnitude

0

ClinVar
Risk	rs786205892(T;T)
Alt	rs786205892(T;T)
Reference	Rs786205892(A;A)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153357667T>A
CLNSRC
CLNACC	RCV000172861.1,