rs786205019

Orientation

minus

Stabilized

minus

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

Make rs786205019(ACCTCCACCTGAGCCCGAGAG;CTGAGCCCCAGGACTTGAGCA)

Make rs786205019(CTGAGCCCCAGGACTTGAGCA;CTGAGCCCCAGGACTTGAGCA)

Reference

GRCh38.p2 38.2/146

Chromosome

X

Position

154030644

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs786205019
dbSNP (classic)	rs786205019
ClinGen	rs786205019
ebi	rs786205019
HLI	rs786205019
Exac	rs786205019
Gnomad	rs786205019
Varsome	rs786205019
LitVar	rs786205019
Map	rs786205019
PheGenI	rs786205019
Biobank	rs786205019
1000 genomes	rs786205019
hgdp	rs786205019
ensembl	rs786205019
geneview	rs786205019
scholar	rs786205019
google	rs786205019
pharmgkb	rs786205019
gwascentral	rs786205019
openSNP	rs786205019
23andMe	rs786205019
SNPshot	rs786205019
SNPdbe	rs786205019
MSV3d	rs786205019
GWAS Ctlg	rs786205019

Max Magnitude

0

ClinVar
Risk	rs786205019(CTGAGCCCCAGGACTTGAGCA;CTGAGCCCCAGGACTTGAGCA)
Alt	rs786205019(CTGAGCCCCAGGACTTGAGCA;CTGAGCCCCAGGACTTGAGCA)
Reference	Rs786205019(ACCTCCACCTGAGCCCGAGAG;ACCTCCACCTGAGCCCGAGAG)
Significance	Pathogenic
Disease	Attention deficit hyperactivity disorder Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Attention deficit hyperactivity disorder Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153296095_153296115del21insTGCTCAAGTCCTGGGGCTCAG
CLNSRC
CLNACC	RCV000170149.1, RCV000170150.1,