rs193922677

Orientation

minus

Stabilized

minus

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

Make rs193922677(A;A)

Make rs193922677(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

154030501

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs193922677
dbSNP (classic)	rs193922677
ClinGen	rs193922677
ebi	rs193922677
HLI	rs193922677
Exac	rs193922677
Gnomad	rs193922677
Varsome	rs193922677
LitVar	rs193922677
Map	rs193922677
PheGenI	rs193922677
Biobank	rs193922677
1000 genomes	rs193922677
hgdp	rs193922677
ensembl	rs193922677
geneview	rs193922677
scholar	rs193922677
google	rs193922677
pharmgkb	rs193922677
gwascentral	rs193922677
openSNP	rs193922677
23andMe	rs193922677
SNPshot	rs193922677
SNPdbe	rs193922677
MSV3d	rs193922677
GWAS Ctlg	rs193922677

Max Magnitude

0

ClinVar
Risk	rs193922677(A;A)
Alt	rs193922677(A;A)
Reference	Rs193922677(G;G)
Significance	Probable-non-pathogenic
Disease	Rett syndrome Mental retardation not provided not specified
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome Mental retardation, X-linked, syndromic 13 not provided not specified
Reversed	1
HGVS	NC_000023.10:g.153295952C>T
CLNSRC	ClinVar LabCorp
CLNACC	RCV000030163.1, RCV000170261.1, RCV000415982.1, RCV000438624.1,