rs267608599

Merged into

rs267608589

Orientation

minus

Stabilized

minus

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

Make rs267608599(-;-)

Make rs267608599(-;CACCTCCACCTGAGCCCGAGAGCTCCGAGGACCCC)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154030631

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608599
dbSNP (classic)	rs267608599
ClinGen	rs267608599
ebi	rs267608599
HLI	rs267608599
Exac	rs267608599
Gnomad	rs267608599
Varsome	rs267608599
LitVar	rs267608599
Map	rs267608599
PheGenI	rs267608599
Biobank	rs267608599
1000 genomes	rs267608599
hgdp	rs267608599
ensembl	rs267608599
geneview	rs267608599
scholar	rs267608599
google	rs267608599
pharmgkb	rs267608599
gwascentral	rs267608599
openSNP	rs267608599
23andMe	rs267608599
SNPshot	rs267608599
SNPdbe	rs267608599
MSV3d	rs267608599
GWAS Ctlg	rs267608599

Status

Merged into rs267608589

Max Magnitude

0

ClinVar
Risk
Alt
Reference	Rs267608599(CACCTCCACCTGAGCCCGAGAGCTCCGAGGACCCC;CACCTCCACCTGAGCCCGAGAGCTCCGAGGACCCC)
Significance	Pathogenic
Disease	not provided Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	not provided Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153296082_153296116del35
CLNSRC
CLNACC	RCV000132906.1, RCV000132928.2,