rs786205038

Orientation

minus

Stabilized

minus

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

Make rs786205038(-;CGCCG)

Make rs786205038(CGCCG;CGCCG)

Reference

GRCh38.p2 38.2/146

Chromosome

X

Position

154097638

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs786205038
dbSNP (classic)	rs786205038
ClinGen	rs786205038
ebi	rs786205038
HLI	rs786205038
Exac	rs786205038
Gnomad	rs786205038
Varsome	rs786205038
LitVar	rs786205038
Map	rs786205038
PheGenI	rs786205038
Biobank	rs786205038
1000 genomes	rs786205038
hgdp	rs786205038
ensembl	rs786205038
geneview	rs786205038
scholar	rs786205038
google	rs786205038
pharmgkb	rs786205038
gwascentral	rs786205038
openSNP	rs786205038
23andMe	rs786205038
SNPshot	rs786205038
SNPdbe	rs786205038
MSV3d	rs786205038
GWAS Ctlg	rs786205038

Max Magnitude

0

ClinVar
Risk	rs786205038(CGCCG;CGCCG)
Alt	rs786205038(CGCCG;CGCCG)
Reference	Rs786205038(-;-)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153363096_153363100dupCGGCG
CLNSRC
CLNACC	RCV000170282.1,