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rs267608487

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267608487(-;-)
Make rs267608487(-;A)
Make rs267608487(A;A)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031343
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608487
ebirs267608487
HLIrs267608487
Exacrs267608487
Varsomers267608487
Maprs267608487
PheGenIrs267608487
hapmaprs267608487
1000 genomesrs267608487
hgdprs267608487
ensemblrs267608487
gopubmedrs267608487
geneviewrs267608487
scholarrs267608487
googlers267608487
pharmgkbrs267608487
gwascentralrs267608487
openSNPrs267608487
23andMers267608487
23andMe allrs267608487
SNP Nexus

SNPshotrs267608487
SNPdbers267608487
MSV3drs267608487
GWAS Ctlgrs267608487
Max Magnitude0
ClinVar
Risk rs267608487(A;A)
Alt rs267608487(A;A)
Reference rs267608487(;)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296795dupT
CLNSRC
CLNACC RCV000133139.2,