rs267608550

Orientation

minus

Stabilized

minus

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

Make rs267608550(A;G)

Make rs267608550(G;G)

Reference

GRCh38 38.1/142

Chromosome

X

Position

154030917

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608550
dbSNP (classic)	rs267608550
ClinGen	rs267608550
ebi	rs267608550
HLI	rs267608550
Exac	rs267608550
Gnomad	rs267608550
Varsome	rs267608550
LitVar	rs267608550
Map	rs267608550
PheGenI	rs267608550
Biobank	rs267608550
1000 genomes	rs267608550
hgdp	rs267608550
ensembl	rs267608550
geneview	rs267608550
scholar	rs267608550
google	rs267608550
pharmgkb	rs267608550
gwascentral	rs267608550
openSNP	rs267608550
23andMe	rs267608550
SNPshot	rs267608550
SNPdbe	rs267608550
MSV3d	rs267608550
GWAS Ctlg	rs267608550

Max Magnitude

0

ClinVar
Risk	rs267608550(C;C) rs267608550(G;G)
Alt	rs267608550(C;C) rs267608550(G;G)
Reference	Rs267608550(A;A)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	MECP2
CLNDBN	not specified
Reversed	1
HGVS	NC_000023.10:g.153296368T>C
CLNSRC	ClinVar GeneDx
CLNACC	RCV000133287.3,