rs786205042

Orientation

minus

Stabilized

minus

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

Make rs786205042(-;-)

Make rs786205042(-;GCGAGGAGGAG)

Reference

GRCh38.p2 38.2/146

Chromosome

X

Position

154097609

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs786205042
dbSNP (classic)	rs786205042
ClinGen	rs786205042
ebi	rs786205042
HLI	rs786205042
Exac	rs786205042
Gnomad	rs786205042
Varsome	rs786205042
LitVar	rs786205042
Map	rs786205042
PheGenI	rs786205042
Biobank	rs786205042
1000 genomes	rs786205042
hgdp	rs786205042
ensembl	rs786205042
geneview	rs786205042
scholar	rs786205042
google	rs786205042
pharmgkb	rs786205042
gwascentral	rs786205042
openSNP	rs786205042
23andMe	rs786205042
SNPshot	rs786205042
SNPdbe	rs786205042
MSV3d	rs786205042
GWAS Ctlg	rs786205042

Max Magnitude

0

ClinVar
Risk	rs786205042(-;-)
Alt	rs786205042(-;-)
Reference	Rs786205042(GCGAGGAGGAG;GCGAGGAGGAG)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153363066_153363076delCTCCTCCTCGC
CLNSRC
CLNACC	RCV000170288.1,