rs267608531

Orientation

minus

Stabilized

minus

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

Make rs267608531(-;A)

Make rs267608531(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154030973

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608531
dbSNP (classic)	rs267608531
ClinGen	rs267608531
ebi	rs267608531
HLI	rs267608531
Exac	rs267608531
Gnomad	rs267608531
Varsome	rs267608531
LitVar	rs267608531
Map	rs267608531
PheGenI	rs267608531
Biobank	rs267608531
1000 genomes	rs267608531
hgdp	rs267608531
ensembl	rs267608531
geneview	rs267608531
scholar	rs267608531
google	rs267608531
pharmgkb	rs267608531
gwascentral	rs267608531
openSNP	rs267608531
23andMe	rs267608531
SNPshot	rs267608531
SNPdbe	rs267608531
MSV3d	rs267608531
GWAS Ctlg	rs267608531

Max Magnitude

0

ClinVar
Risk	rs267608531(A;A)
Alt	rs267608531(A;A)
Reference	Rs267608531(-;-)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MECP2
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.153296425dupT
CLNSRC
CLNACC	RCV000133255.2,