rs179363901

Orientation

minus

Stabilized

minus

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

Make rs179363901(C;T)

Make rs179363901(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

154097661

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs179363901
dbSNP (classic)	rs179363901
ClinGen	rs179363901
ebi	rs179363901
HLI	rs179363901
Exac	rs179363901
Gnomad	rs179363901
Varsome	rs179363901
LitVar	rs179363901
Map	rs179363901
PheGenI	rs179363901
Biobank	rs179363901
1000 genomes	rs179363901
hgdp	rs179363901
ensembl	rs179363901
geneview	rs179363901
scholar	rs179363901
google	rs179363901
pharmgkb	rs179363901
gwascentral	rs179363901
openSNP	rs179363901
23andMe	rs179363901
SNPshot	rs179363901
SNPdbe	rs179363901
MSV3d	rs179363901
GWAS Ctlg	rs179363901

Max Magnitude

0

ClinVar
Risk	rs179363901(T;T)
Alt	rs179363901(T;T)
Reference	Rs179363901(C;C)
Significance	Other
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153363118G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000012619.27,