rs61754419

Orientation

minus

Stabilized

minus

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

Make rs61754419(-;-)

Make rs61754419(-;TGCCCCCACCTCCACCTGAGCCCGAGAGCTC)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154030641

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs61754419
dbSNP (classic)	rs61754419
ClinGen	rs61754419
ebi	rs61754419
HLI	rs61754419
Exac	rs61754419
Gnomad	rs61754419
Varsome	rs61754419
LitVar	rs61754419
Map	rs61754419
PheGenI	rs61754419
Biobank	rs61754419
1000 genomes	rs61754419
hgdp	rs61754419
ensembl	rs61754419
geneview	rs61754419
scholar	rs61754419
google	rs61754419
pharmgkb	rs61754419
gwascentral	rs61754419
openSNP	rs61754419
23andMe	rs61754419
SNPshot	rs61754419
SNPdbe	rs61754419
MSV3d	rs61754419
GWAS Ctlg	rs61754419

Max Magnitude

0

ClinVar
Risk	rs61754419(-;-)
Alt	rs61754419(-;-)
Reference	Rs61754419(TGCCCCCACCTCCACCTGAGCCCGAGAGCTC;TGCCCCCACCTCCACCTGAGCCCGAGAGCTC)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153296092_153296122del31
CLNSRC
CLNACC	RCV000132891.2,