rs587783095

Orientation

minus

Stabilized

minus

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

Make rs587783095(-;C)

Make rs587783095(C;C)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154030537

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs587783095
dbSNP (classic)	rs587783095
ClinGen	rs587783095
ebi	rs587783095
HLI	rs587783095
Exac	rs587783095
Gnomad	rs587783095
Varsome	rs587783095
LitVar	rs587783095
Map	rs587783095
PheGenI	rs587783095
Biobank	rs587783095
1000 genomes	rs587783095
hgdp	rs587783095
ensembl	rs587783095
geneview	rs587783095
scholar	rs587783095
google	rs587783095
pharmgkb	rs587783095
gwascentral	rs587783095
openSNP	rs587783095
23andMe	rs587783095
SNPshot	rs587783095
SNPdbe	rs587783095
MSV3d	rs587783095
GWAS Ctlg	rs587783095

Max Magnitude

0

ClinVar
Risk	rs587783095(C;C)
Alt	rs587783095(C;C)
Reference	Rs587783095(-;-)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MECP2
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.153295989dupG
CLNSRC
CLNACC	RCV000144761.1,