rs61754438

Orientation

minus

Stabilized

minus

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

Make rs61754438(-;-)

Make rs61754438(-;G)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154032383

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs61754438
dbSNP (classic)	rs61754438
ClinGen	rs61754438
ebi	rs61754438
HLI	rs61754438
Exac	rs61754438
Gnomad	rs61754438
Varsome	rs61754438
LitVar	rs61754438
Map	rs61754438
PheGenI	rs61754438
Biobank	rs61754438
1000 genomes	rs61754438
hgdp	rs61754438
ensembl	rs61754438
geneview	rs61754438
scholar	rs61754438
google	rs61754438
pharmgkb	rs61754438
gwascentral	rs61754438
openSNP	rs61754438
23andMe	rs61754438
SNPshot	rs61754438
SNPdbe	rs61754438
MSV3d	rs61754438
GWAS Ctlg	rs61754438

Max Magnitude

0

ClinVar
Risk	rs61754438(-;-)
Alt	rs61754438(-;-)
Reference	Rs61754438(G;G)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153297834delC
CLNSRC
CLNACC	RCV000133030.2,