rs193922679

Orientation

minus

Stabilized

minus

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

Make rs193922679(A;T)

Make rs193922679(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

154031254

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs193922679
dbSNP (classic)	rs193922679
ClinGen	rs193922679
ebi	rs193922679
HLI	rs193922679
Exac	rs193922679
Gnomad	rs193922679
Varsome	rs193922679
LitVar	rs193922679
Map	rs193922679
PheGenI	rs193922679
Biobank	rs193922679
1000 genomes	rs193922679
hgdp	rs193922679
ensembl	rs193922679
geneview	rs193922679
scholar	rs193922679
google	rs193922679
pharmgkb	rs193922679
gwascentral	rs193922679
openSNP	rs193922679
23andMe	rs193922679
SNPshot	rs193922679
SNPdbe	rs193922679
MSV3d	rs193922679
GWAS Ctlg	rs193922679

Max Magnitude

0

ClinVar
Risk	rs193922679(T;T)
Alt	rs193922679(T;T)
Reference	Rs193922679(A;A)
Significance	Other
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153296705T>A
CLNSRC	ClinVar
CLNACC	RCV000030165.3,