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rs267608613

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267608613(-;-)
Make rs267608613(-;C)
Make rs267608613(C;C)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030627
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608613
ebirs267608613
HLIrs267608613
Exacrs267608613
Varsomers267608613
Maprs267608613
PheGenIrs267608613
hapmaprs267608613
1000 genomesrs267608613
hgdprs267608613
ensemblrs267608613
gopubmedrs267608613
geneviewrs267608613
scholarrs267608613
googlers267608613
pharmgkbrs267608613
gwascentralrs267608613
openSNPrs267608613
23andMers267608613
23andMe allrs267608613
SNP Nexus

SNPshotrs267608613
SNPdbers267608613
MSV3drs267608613
GWAS Ctlgrs267608613
Max Magnitude0
ClinVar
Risk rs267608613(C;C)
Alt rs267608613(C;C)
Reference rs267608613(;)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296079dupG
CLNSRC
CLNACC RCV000132960.2,