Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs267608455

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267608455(A;A)
Make rs267608455(A;G)
ReferenceGRCh38.p7 38.3/149
ChromosomeX
Position154032220
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608455
dbSNP (old)rs267608455
ClinGenrs267608455
ebirs267608455
HLIrs267608455
Exacrs267608455
Gnomadrs267608455
Varsomers267608455
Maprs267608455
PheGenIrs267608455
Biobankrs267608455
1000 genomesrs267608455
hgdprs267608455
ensemblrs267608455
gopubmedrs267608455
geneviewrs267608455
scholarrs267608455
googlers267608455
pharmgkbrs267608455
gwascentralrs267608455
openSNPrs267608455
23andMers267608455
23andMe allrs267608455
SNPshotrs267608455
SNPdbers267608455
MSV3drs267608455
GWAS Ctlgrs267608455
Max Magnitude0
ClinVar
Risk rs267608455(A;A)
Alt rs267608455(A;A)
Reference Rs267608455(G;G)
Significance Pathogenic
Disease Rett syndrome not provided
Variation info
Gene MECP2
CLNDBN Rett syndrome not provided
Reversed 1
HGVS NC_000023.10:g.153297671C>T
CLNSRC
CLNACC RCV000133079.2, RCV000254852.1,