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rs267608582

From SNPedia

Orientationminus
Geno Mag Summary
(CTGCCCCCACCTCCACC;CTGCCCCCACCTCCACC) 0 common in clinvar
Make rs267608582(-;-)
Make rs267608582(-;CTGCCCCCACCTCCACC)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030656
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608582
ebirs267608582
HLIrs267608582
Exacrs267608582
Varsomers267608582
Maprs267608582
PheGenIrs267608582
hapmaprs267608582
1000 genomesrs267608582
hgdprs267608582
ensemblrs267608582
gopubmedrs267608582
geneviewrs267608582
scholarrs267608582
googlers267608582
pharmgkbrs267608582
gwascentralrs267608582
openSNPrs267608582
23andMers267608582
23andMe allrs267608582
SNP Nexus

SNPshotrs267608582
SNPdbers267608582
MSV3drs267608582
GWAS Ctlgrs267608582
Max Magnitude0
ClinVar
Risk rs267608582(;)
Alt rs267608582(;)
Reference rs267608582(CTGCCCCCACCTCCACC;CTGCCCCCACCTCCACC)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296107_153296123del17
CLNSRC
CLNACC RCV000132888.2,