rs61754436

Orientation

minus

Stabilized

minus

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

Make rs61754436(-;-)

Make rs61754436(-;GA)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154032394

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs61754436
dbSNP (classic)	rs61754436
ClinGen	rs61754436
ebi	rs61754436
HLI	rs61754436
Exac	rs61754436
Gnomad	rs61754436
Varsome	rs61754436
LitVar	rs61754436
Map	rs61754436
PheGenI	rs61754436
Biobank	rs61754436
1000 genomes	rs61754436
hgdp	rs61754436
ensembl	rs61754436
geneview	rs61754436
scholar	rs61754436
google	rs61754436
pharmgkb	rs61754436
gwascentral	rs61754436
openSNP	rs61754436
23andMe	rs61754436
SNPshot	rs61754436
SNPdbe	rs61754436
MSV3d	rs61754436
GWAS Ctlg	rs61754436

Max Magnitude

0

ClinVar
Risk	rs61754436(-;-)
Alt	rs61754436(-;-)
Reference	Rs61754436(GA;GA)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153297845_153297846delTC
CLNSRC
CLNACC	RCV000133028.2,