rs61748428

Orientation

minus

Stabilized

minus

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

Make rs61748428(A;T)

Make rs61748428(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154031305

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs61748428
dbSNP (classic)	rs61748428
ClinGen	rs61748428
ebi	rs61748428
HLI	rs61748428
Exac	rs61748428
Gnomad	rs61748428
Varsome	rs61748428
LitVar	rs61748428
Map	rs61748428
PheGenI	rs61748428
Biobank	rs61748428
1000 genomes	rs61748428
hgdp	rs61748428
ensembl	rs61748428
geneview	rs61748428
scholar	rs61748428
google	rs61748428
pharmgkb	rs61748428
gwascentral	rs61748428
openSNP	rs61748428
23andMe	rs61748428
SNPshot	rs61748428
SNPdbe	rs61748428
MSV3d	rs61748428
GWAS Ctlg	rs61748428

Max Magnitude

0

ClinVar
Risk	rs61748428(T;T)
Alt	rs61748428(T;T)
Reference	Rs61748428(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MECP2
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.153296756T>A
CLNSRC
CLNACC	RCV000133150.2,