rs587783092

Orientation

minus

Stabilized

minus

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

Make rs587783092(-;-)

Make rs587783092(-;C)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154030742

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs587783092
dbSNP (classic)	rs587783092
ClinGen	rs587783092
ebi	rs587783092
HLI	rs587783092
Exac	rs587783092
Gnomad	rs587783092
Varsome	rs587783092
LitVar	rs587783092
Map	rs587783092
PheGenI	rs587783092
Biobank	rs587783092
1000 genomes	rs587783092
hgdp	rs587783092
ensembl	rs587783092
geneview	rs587783092
scholar	rs587783092
google	rs587783092
pharmgkb	rs587783092
gwascentral	rs587783092
openSNP	rs587783092
23andMe	rs587783092
SNPshot	rs587783092
SNPdbe	rs587783092
MSV3d	rs587783092
GWAS Ctlg	rs587783092

Max Magnitude

0

ClinVar
Risk	rs587783092(-;-)
Alt	rs587783092(-;-)
Reference	Rs587783092(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MECP2
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.153296193delG
CLNSRC
CLNACC	RCV000144755.1,