rs179363900

Orientation

minus

Stabilized

minus

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

Make rs179363900(C;G)

Make rs179363900(G;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

154031374

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs179363900
dbSNP (classic)	rs179363900
ClinGen	rs179363900
ebi	rs179363900
HLI	rs179363900
Exac	rs179363900
Gnomad	rs179363900
Varsome	rs179363900
LitVar	rs179363900
Map	rs179363900
PheGenI	rs179363900
Biobank	rs179363900
1000 genomes	rs179363900
hgdp	rs179363900
ensembl	rs179363900
geneview	rs179363900
scholar	rs179363900
google	rs179363900
pharmgkb	rs179363900
gwascentral	rs179363900
openSNP	rs179363900
23andMe	rs179363900
SNPshot	rs179363900
SNPdbe	rs179363900
MSV3d	rs179363900
GWAS Ctlg	rs179363900

Max Magnitude

0

ClinVar
Risk	rs179363900(G;G)
Alt	rs179363900(G;G)
Reference	Rs179363900(C;C)
Significance	Pathogenic
Disease	Rett syndrome Mental retardation not provided
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome, zappella variant Mental retardation, X-linked, syndromic 13 not provided
Reversed	1
HGVS	NC_000023.10:g.153296825G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000012618.24, RCV000133115.2, RCV000492792.1,