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rs267608486

From SNPedia

Orientationminus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs267608486(-;-)
Make rs267608486(-;TG)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031347
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608486
ebirs267608486
HLIrs267608486
Exacrs267608486
Varsomers267608486
Maprs267608486
PheGenIrs267608486
hapmaprs267608486
1000 genomesrs267608486
hgdprs267608486
ensemblrs267608486
gopubmedrs267608486
geneviewrs267608486
scholarrs267608486
googlers267608486
pharmgkbrs267608486
gwascentralrs267608486
openSNPrs267608486
23andMers267608486
23andMe allrs267608486
SNP Nexus

SNPshotrs267608486
SNPdbers267608486
MSV3drs267608486
GWAS Ctlgrs267608486
Max Magnitude0
ClinVar
Risk rs267608486(;)
Alt rs267608486(;)
Reference rs267608486(TG;TG)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296798_153296799delCA
CLNSRC
CLNACC RCV000133133.2,