rs61754430

Orientation

minus

Stabilized

minus

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

Make rs61754430(-;G)

Make rs61754430(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154032457

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs61754430
dbSNP (classic)	rs61754430
ClinGen	rs61754430
ebi	rs61754430
HLI	rs61754430
Exac	rs61754430
Gnomad	rs61754430
Varsome	rs61754430
LitVar	rs61754430
Map	rs61754430
PheGenI	rs61754430
Biobank	rs61754430
1000 genomes	rs61754430
hgdp	rs61754430
ensembl	rs61754430
geneview	rs61754430
scholar	rs61754430
google	rs61754430
pharmgkb	rs61754430
gwascentral	rs61754430
openSNP	rs61754430
23andMe	rs61754430
SNPshot	rs61754430
SNPdbe	rs61754430
MSV3d	rs61754430
GWAS Ctlg	rs61754430

Max Magnitude

0

ClinVar
Risk	rs61754430(G;G)
Alt	rs61754430(G;G)
Reference	Rs61754430(-;-)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153297909dupC
CLNSRC
CLNACC	RCV000132980.2,