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rs267608449

From SNPedia

Orientationminus
Geno Mag Summary
(ACC;ACC) 0 common in clinvar
Make rs267608449(-;-)
Make rs267608449(-;ACC)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154032287
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608449
ebirs267608449
HLIrs267608449
Exacrs267608449
Varsomers267608449
Maprs267608449
PheGenIrs267608449
hapmaprs267608449
1000 genomesrs267608449
hgdprs267608449
ensemblrs267608449
gopubmedrs267608449
geneviewrs267608449
scholarrs267608449
googlers267608449
pharmgkbrs267608449
gwascentralrs267608449
openSNPrs267608449
23andMers267608449
23andMe allrs267608449
SNP Nexus

SNPshotrs267608449
SNPdbers267608449
MSV3drs267608449
GWAS Ctlgrs267608449
Max Magnitude0
ClinVar
Risk rs267608449(;)
Alt rs267608449(;)
Reference rs267608449(ACC;ACC)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153297738_153297740delGGT
CLNSRC
CLNACC RCV000133052.2,