rs1064792898

Orientation

minus

Stabilized

minus

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

Chromosome

X

Position

154030699

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs1064792898
dbSNP (classic)	rs1064792898
ClinGen	rs1064792898
ebi	rs1064792898
HLI	rs1064792898
Exac	rs1064792898
Gnomad	rs1064792898
Varsome	rs1064792898
LitVar	rs1064792898
Map	rs1064792898
PheGenI	rs1064792898
Biobank	rs1064792898
1000 genomes	rs1064792898
hgdp	rs1064792898
ensembl	rs1064792898
geneview	rs1064792898
scholar	rs1064792898
google	rs1064792898
pharmgkb	rs1064792898
gwascentral	rs1064792898
openSNP	rs1064792898
23andMe	rs1064792898
SNPshot	rs1064792898
SNPdbe	rs1064792898
MSV3d	rs1064792898
GWAS Ctlg	rs1064792898

Max Magnitude

0

ClinVar
Risk	rs1064792898(-;-)
Alt	rs1064792898(-;-)
Reference	Rs1064792898(GAAGGAGCACCACCACCATCACCACCACTCAGAGTCCCCAA;GAAGGAGCACCACCACCATCACCACCACTCAGAGTCCCCAA)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153296150_153296190del41
CLNSRC
CLNACC	RCV000445572.1,