rs267608496

Orientation

minus

Stabilized

minus

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

Make rs267608496(-;-)

Make rs267608496(-;TC)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154031284

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608496
dbSNP (classic)	rs267608496
ClinGen	rs267608496
ebi	rs267608496
HLI	rs267608496
Exac	rs267608496
Gnomad	rs267608496
Varsome	rs267608496
LitVar	rs267608496
Map	rs267608496
PheGenI	rs267608496
Biobank	rs267608496
1000 genomes	rs267608496
hgdp	rs267608496
ensembl	rs267608496
geneview	rs267608496
scholar	rs267608496
google	rs267608496
pharmgkb	rs267608496
gwascentral	rs267608496
openSNP	rs267608496
23andMe	rs267608496
SNPshot	rs267608496
SNPdbe	rs267608496
MSV3d	rs267608496
GWAS Ctlg	rs267608496

Max Magnitude

0

ClinVar
Risk	rs267608496(-;-)
Alt	rs267608496(-;-)
Reference	Rs267608496(TC;TC)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153296735_153296736delGA
CLNSRC
CLNACC	RCV000133157.2,