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rs267608584

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267608584(-;-)
Make rs267608584(-;CT)
Make rs267608584(CT;CT)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030670
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608584
ebirs267608584
HLIrs267608584
Exacrs267608584
Varsomers267608584
Maprs267608584
PheGenIrs267608584
hapmaprs267608584
1000 genomesrs267608584
hgdprs267608584
ensemblrs267608584
gopubmedrs267608584
geneviewrs267608584
scholarrs267608584
googlers267608584
pharmgkbrs267608584
gwascentralrs267608584
openSNPrs267608584
23andMers267608584
23andMe allrs267608584
SNP Nexus

SNPshotrs267608584
SNPdbers267608584
MSV3drs267608584
GWAS Ctlgrs267608584
Max Magnitude0
ClinVar
Risk rs267608584(CT;CT)
Alt rs267608584(CT;CT)
Reference rs267608584(;)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296122_153296123dupAG
CLNSRC
CLNACC RCV000132887.2,