rs61749702

Orientation

minus

Stabilized

minus

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

Make rs61749702(A;T)

Make rs61749702(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154031299

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs61749702
dbSNP (classic)	rs61749702
ClinGen	rs61749702
ebi	rs61749702
HLI	rs61749702
Exac	rs61749702
Gnomad	rs61749702
Varsome	rs61749702
LitVar	rs61749702
Map	rs61749702
PheGenI	rs61749702
Biobank	rs61749702
1000 genomes	rs61749702
hgdp	rs61749702
ensembl	rs61749702
geneview	rs61749702
scholar	rs61749702
google	rs61749702
pharmgkb	rs61749702
gwascentral	rs61749702
openSNP	rs61749702
23andMe	rs61749702
SNPshot	rs61749702
SNPdbe	rs61749702
MSV3d	rs61749702
GWAS Ctlg	rs61749702

Max Magnitude

0

ClinVar
Risk	rs61749702(G;G) rs61749702(T;T)
Alt	rs61749702(G;G) rs61749702(T;T)
Reference	Rs61749702(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MECP2
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.153296750T>A
CLNSRC
CLNACC	RCV000133153.2,