rs61750259

Orientation

minus

Stabilized

minus

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

Make rs61750259(A;T)

Make rs61750259(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154030963

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs61750259
dbSNP (classic)	rs61750259
ClinGen	rs61750259
ebi	rs61750259
HLI	rs61750259
Exac	rs61750259
Gnomad	rs61750259
Varsome	rs61750259
LitVar	rs61750259
Map	rs61750259
PheGenI	rs61750259
Biobank	rs61750259
1000 genomes	rs61750259
hgdp	rs61750259
ensembl	rs61750259
geneview	rs61750259
scholar	rs61750259
google	rs61750259
pharmgkb	rs61750259
gwascentral	rs61750259
openSNP	rs61750259
23andMe	rs61750259
SNPshot	rs61750259
SNPdbe	rs61750259
MSV3d	rs61750259
GWAS Ctlg	rs61750259

Max Magnitude

0

ClinVar
Risk	rs61750259(T;T)
Alt	rs61750259(T;T)
Reference	Rs61750259(A;A)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153296414T>A
CLNSRC
CLNACC	RCV000133260.2,