rs63749010

Orientation

minus

Stabilized

minus

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

Make rs63749010(-;-)

Make rs63749010(-;GGACACGGAAGCT)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154032261

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs63749010
dbSNP (classic)	rs63749010
ClinGen	rs63749010
ebi	rs63749010
HLI	rs63749010
Exac	rs63749010
Gnomad	rs63749010
Varsome	rs63749010
LitVar	rs63749010
Map	rs63749010
PheGenI	rs63749010
Biobank	rs63749010
1000 genomes	rs63749010
hgdp	rs63749010
ensembl	rs63749010
geneview	rs63749010
scholar	rs63749010
google	rs63749010
pharmgkb	rs63749010
gwascentral	rs63749010
openSNP	rs63749010
23andMe	rs63749010
SNPshot	rs63749010
SNPdbe	rs63749010
MSV3d	rs63749010
GWAS Ctlg	rs63749010

Max Magnitude

0

ClinVar
Risk	rs63749010(-;-)
Alt	rs63749010(-;-)
Reference	Rs63749010(GGACACGGAAGCT;GGACACGGAAGCT)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153297712_153297724delAGCTTCCGTGTCC
CLNSRC
CLNACC	RCV000133063.2,