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rs267608452

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267608452(-;-)
Make rs267608452(-;A)
Make rs267608452(A;A)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154032257
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608452
ebirs267608452
HLIrs267608452
Exacrs267608452
Varsomers267608452
Maprs267608452
PheGenIrs267608452
hapmaprs267608452
1000 genomesrs267608452
hgdprs267608452
ensemblrs267608452
gopubmedrs267608452
geneviewrs267608452
scholarrs267608452
googlers267608452
pharmgkbrs267608452
gwascentralrs267608452
openSNPrs267608452
23andMers267608452
23andMe allrs267608452
SNP Nexus

SNPshotrs267608452
SNPdbers267608452
MSV3drs267608452
GWAS Ctlgrs267608452
Max Magnitude0
ClinVar
Risk rs267608452(A;A)
Alt rs267608452(A;A)
Reference rs267608452(;)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153297709dupT
CLNSRC
CLNACC RCV000133070.2,