rs61749736

Orientation

minus

Stabilized

minus

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

Make rs61749736(-;A)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154031150

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs61749736
dbSNP (classic)	rs61749736
ClinGen	rs61749736
ebi	rs61749736
HLI	rs61749736
Exac	rs61749736
Gnomad	rs61749736
Varsome	rs61749736
LitVar	rs61749736
Map	rs61749736
PheGenI	rs61749736
Biobank	rs61749736
1000 genomes	rs61749736
hgdp	rs61749736
ensembl	rs61749736
geneview	rs61749736
scholar	rs61749736
google	rs61749736
pharmgkb	rs61749736
gwascentral	rs61749736
openSNP	rs61749736
23andMe	rs61749736
SNPshot	rs61749736
SNPdbe	rs61749736
MSV3d	rs61749736
GWAS Ctlg	rs61749736

Max Magnitude

0

ClinVar
Risk	Rs61749736(A;A)
Alt	Rs61749736(A;A)
Reference	Rs61749736(-;-)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153296601_153296602insT
CLNSRC
CLNACC	RCV000133196.2,