rs267608597

Orientation

minus

Stabilized

minus

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

Make rs267608597(CC;TA)

Make rs267608597(TA;TA)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154030665

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs267608597
dbSNP (classic)	rs267608597
ClinGen	rs267608597
ebi	rs267608597
HLI	rs267608597
Exac	rs267608597
Gnomad	rs267608597
Varsome	rs267608597
LitVar	rs267608597
Map	rs267608597
PheGenI	rs267608597
Biobank	rs267608597
1000 genomes	rs267608597
hgdp	rs267608597
ensembl	rs267608597
geneview	rs267608597
scholar	rs267608597
google	rs267608597
pharmgkb	rs267608597
gwascentral	rs267608597
openSNP	rs267608597
23andMe	rs267608597
SNPshot	rs267608597
SNPdbe	rs267608597
MSV3d	rs267608597
GWAS Ctlg	rs267608597

Max Magnitude

0

ClinVar
Risk	rs267608597(TA;TA)
Alt	rs267608597(TA;TA)
Reference	Rs267608597(CC;CC)
Significance	Pathogenic
Disease	Mental retardation
Variation	info
Gene	MECP2
CLNDBN	Mental retardation, X-linked, syndromic 13
Reversed	1
HGVS	NC_000023.10:g.153296116_153296117delGGinsTA
CLNSRC
CLNACC	RCV000132921.2,