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rs267608523

From SNPedia

Orientationminus
Geno Mag Summary
(CAGG;CAGG) 0 common in clinvar
Make rs267608523(-;-)
Make rs267608523(-;CAGG)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031069
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608523
ebirs267608523
HLIrs267608523
Exacrs267608523
Varsomers267608523
Maprs267608523
PheGenIrs267608523
hapmaprs267608523
1000 genomesrs267608523
hgdprs267608523
ensemblrs267608523
gopubmedrs267608523
geneviewrs267608523
scholarrs267608523
googlers267608523
pharmgkbrs267608523
gwascentralrs267608523
openSNPrs267608523
23andMers267608523
23andMe allrs267608523
SNP Nexus

SNPshotrs267608523
SNPdbers267608523
MSV3drs267608523
GWAS Ctlgrs267608523
Max Magnitude0
ClinVar
Risk rs267608523(;)
Alt rs267608523(;)
Reference rs267608523(CAGG;CAGG)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296520_153296523delCCTG
CLNSRC
CLNACC RCV000133232.2,