rs587783090

Orientation

minus

Stabilized

minus

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

Make rs587783090(-;-)

Make rs587783090(-;G)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154032309

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs587783090
dbSNP (classic)	rs587783090
ClinGen	rs587783090
ebi	rs587783090
HLI	rs587783090
Exac	rs587783090
Gnomad	rs587783090
Varsome	rs587783090
LitVar	rs587783090
Map	rs587783090
PheGenI	rs587783090
Biobank	rs587783090
1000 genomes	rs587783090
hgdp	rs587783090
ensembl	rs587783090
geneview	rs587783090
scholar	rs587783090
google	rs587783090
pharmgkb	rs587783090
gwascentral	rs587783090
openSNP	rs587783090
23andMe	rs587783090
SNPshot	rs587783090
SNPdbe	rs587783090
MSV3d	rs587783090
GWAS Ctlg	rs587783090

Max Magnitude

0

ClinVar
Risk	rs587783090(-;-)
Alt	rs587783090(-;-)
Reference	Rs587783090(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MECP2
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.153297760delC
CLNSRC
CLNACC	RCV000144752.1,