rs61752375

Orientation

minus

Stabilized

minus

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

Make rs61752375(A;T)

Make rs61752375(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154030741

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs61752375
dbSNP (classic)	rs61752375
ClinGen	rs61752375
ebi	rs61752375
HLI	rs61752375
Exac	rs61752375
Gnomad	rs61752375
Varsome	rs61752375
LitVar	rs61752375
Map	rs61752375
PheGenI	rs61752375
Biobank	rs61752375
1000 genomes	rs61752375
hgdp	rs61752375
ensembl	rs61752375
geneview	rs61752375
scholar	rs61752375
google	rs61752375
pharmgkb	rs61752375
gwascentral	rs61752375
openSNP	rs61752375
23andMe	rs61752375
SNPshot	rs61752375
SNPdbe	rs61752375
MSV3d	rs61752375
GWAS Ctlg	rs61752375

Max Magnitude

0

ClinVar
Risk	rs61752375(T;T)
Alt	rs61752375(T;T)
Reference	Rs61752375(A;A)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153296192T>A
CLNSRC
CLNACC	RCV000132851.2,