rs63094662

Orientation

minus

Stabilized

minus

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

Make rs63094662(A;A)

Make rs63094662(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

154030648

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs63094662
dbSNP (classic)	rs63094662
ClinGen	rs63094662
ebi	rs63094662
HLI	rs63094662
Exac	rs63094662
Gnomad	rs63094662
Varsome	rs63094662
LitVar	rs63094662
Map	rs63094662
PheGenI	rs63094662
Biobank	rs63094662
1000 genomes	rs63094662
hgdp	rs63094662
ensembl	rs63094662
geneview	rs63094662
scholar	rs63094662
google	rs63094662
pharmgkb	rs63094662
gwascentral	rs63094662
openSNP	rs63094662
23andMe	rs63094662
SNPshot	rs63094662
SNPdbe	rs63094662
MSV3d	rs63094662
GWAS Ctlg	rs63094662

Max Magnitude

0

ClinVar
Risk	rs63094662(A;A) rs63094662(T;T)
Alt	rs63094662(A;A) rs63094662(T;T)
Reference	Rs63094662(G;G)
Significance	Other
Disease	Mental retardation Rett syndrome not specified
Variation	info
Gene	MECP2
CLNDBN	Mental retardation, X-linked, syndromic 13 Rett syndrome not specified
Reversed	1
HGVS	NC_000023.10:g.153296099C>A; NC_000023.10:g.153296099C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000012588.22, RCV000146349.1, RCV000132947.3, RCV000445563.1,