rs28935168

Orientation

minus

Stabilized

minus

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

Make rs28935168(C;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

154032286

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs28935168
dbSNP (classic)	rs28935168
ClinGen	rs28935168
ebi	rs28935168
HLI	rs28935168
Exac	rs28935168
Gnomad	rs28935168
Varsome	rs28935168
LitVar	rs28935168
Map	rs28935168
PheGenI	rs28935168
Biobank	rs28935168
1000 genomes	rs28935168
hgdp	rs28935168
ensembl	rs28935168
geneview	rs28935168
scholar	rs28935168
google	rs28935168
pharmgkb	rs28935168
gwascentral	rs28935168
openSNP	rs28935168
23andMe	rs28935168
SNPshot	rs28935168
SNPdbe	rs28935168
MSV3d	rs28935168
GWAS Ctlg	rs28935168

Max Magnitude

0

OMIM	300005
Desc	RETT SYNDROME
Variant	0027
Related	also

ClinVar
Risk	Rs28935168(G;G)
Alt	Rs28935168(G;G)
Reference	Rs28935168(C;C)
Significance	Other
Disease	Rett syndrome not specified
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome not specified
Reversed	1
HGVS	NC_000023.10:g.153297737G>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000012608.23, RCV000168679.2,