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rs267608529

From SNPedia

Orientationminus
Geno Mag Summary
(AAAG;AAAG) 0 common in clinvar
Make rs267608529(-;-)
Make rs267608529(-;AAAG)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031015
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608529
ebirs267608529
HLIrs267608529
Exacrs267608529
Varsomers267608529
Maprs267608529
PheGenIrs267608529
hapmaprs267608529
1000 genomesrs267608529
hgdprs267608529
ensemblrs267608529
gopubmedrs267608529
geneviewrs267608529
scholarrs267608529
googlers267608529
pharmgkbrs267608529
gwascentralrs267608529
openSNPrs267608529
23andMers267608529
23andMe allrs267608529
SNP Nexus

SNPshotrs267608529
SNPdbers267608529
MSV3drs267608529
GWAS Ctlgrs267608529
Max Magnitude0
ClinVar
Risk rs267608529(;)
Alt rs267608529(;)
Reference rs267608529(AAAG;AAAG)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296466_153296469delCTTT
CLNSRC
CLNACC RCV000133244.2,