rs267608641

Orientation

minus

Stabilized

minus

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

Make rs267608641(-;TA)

Make rs267608641(TA;TA)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154030371

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608641
dbSNP (classic)	rs267608641
ClinGen	rs267608641
ebi	rs267608641
HLI	rs267608641
Exac	rs267608641
Gnomad	rs267608641
Varsome	rs267608641
LitVar	rs267608641
Map	rs267608641
PheGenI	rs267608641
Biobank	rs267608641
1000 genomes	rs267608641
hgdp	rs267608641
ensembl	rs267608641
geneview	rs267608641
scholar	rs267608641
google	rs267608641
pharmgkb	rs267608641
gwascentral	rs267608641
openSNP	rs267608641
23andMe	rs267608641
SNPshot	rs267608641
SNPdbe	rs267608641
MSV3d	rs267608641
GWAS Ctlg	rs267608641

Max Magnitude

0

ClinVar
Risk	rs267608641(TA;TA)
Alt	rs267608641(TA;TA)
Reference	Rs267608641(-;-)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153295823_153295824dupTA
CLNSRC
CLNACC	RCV000133017.2,