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rs267608482

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267608482(-;-)
Make rs267608482(-;T)
Make rs267608482(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031357
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608482
ebirs267608482
HLIrs267608482
Exacrs267608482
Varsomers267608482
Maprs267608482
PheGenIrs267608482
hapmaprs267608482
1000 genomesrs267608482
hgdprs267608482
ensemblrs267608482
gopubmedrs267608482
geneviewrs267608482
scholarrs267608482
googlers267608482
pharmgkbrs267608482
gwascentralrs267608482
openSNPrs267608482
23andMers267608482
23andMe allrs267608482
SNP Nexus

SNPshotrs267608482
SNPdbers267608482
MSV3drs267608482
GWAS Ctlgrs267608482
Max Magnitude0
ClinVar
Risk rs267608482(T;T)
Alt rs267608482(T;T)
Reference rs267608482(;)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296809dupA
CLNSRC
CLNACC RCV000133126.2,