rs61754425

Orientation

minus

Stabilized

minus

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

Make rs61754425(C;T)

Make rs61754425(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154032529

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs61754425
dbSNP (classic)	rs61754425
ClinGen	rs61754425
ebi	rs61754425
HLI	rs61754425
Exac	rs61754425
Gnomad	rs61754425
Varsome	rs61754425
LitVar	rs61754425
Map	rs61754425
PheGenI	rs61754425
Biobank	rs61754425
1000 genomes	rs61754425
hgdp	rs61754425
ensembl	rs61754425
geneview	rs61754425
scholar	rs61754425
google	rs61754425
pharmgkb	rs61754425
gwascentral	rs61754425
openSNP	rs61754425
23andMe	rs61754425
SNPshot	rs61754425
SNPdbe	rs61754425
MSV3d	rs61754425
GWAS Ctlg	rs61754425

Max Magnitude

0

ClinVar
Risk	rs61754425(T;T)
Alt	rs61754425(T;T)
Reference	Rs61754425(C;C)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153297980G>A
CLNSRC
CLNACC	RCV000133160.2,