rs1057518568

Orientation

minus

Stabilized

minus

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

Make rs1057518568(-;-)

Make rs1057518568(-;C)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

154031013

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs1057518568
dbSNP (classic)	rs1057518568
ClinGen	rs1057518568
ebi	rs1057518568
HLI	rs1057518568
Exac	rs1057518568
Gnomad	rs1057518568
Varsome	rs1057518568
LitVar	rs1057518568
Map	rs1057518568
PheGenI	rs1057518568
Biobank	rs1057518568
1000 genomes	rs1057518568
hgdp	rs1057518568
ensembl	rs1057518568
geneview	rs1057518568
scholar	rs1057518568
google	rs1057518568
pharmgkb	rs1057518568
gwascentral	rs1057518568
openSNP	rs1057518568
23andMe	rs1057518568
SNPshot	rs1057518568
SNPdbe	rs1057518568
MSV3d	rs1057518568
GWAS Ctlg	rs1057518568

Max Magnitude

0

ClinVar
Risk	rs1057518568(-;-)
Alt	rs1057518568(-;-)
Reference	Rs1057518568(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MECP2
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.153296464delG
CLNSRC
CLNACC	RCV000413774.1,