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rs267608548

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267608548(-;-)
Make rs267608548(-;C)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030922
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608548
ebirs267608548
HLIrs267608548
Exacrs267608548
Varsomers267608548
Maprs267608548
PheGenIrs267608548
hapmaprs267608548
1000 genomesrs267608548
hgdprs267608548
ensemblrs267608548
gopubmedrs267608548
geneviewrs267608548
scholarrs267608548
googlers267608548
pharmgkbrs267608548
gwascentralrs267608548
openSNPrs267608548
23andMers267608548
23andMe allrs267608548
SNP Nexus

SNPshotrs267608548
SNPdbers267608548
MSV3drs267608548
GWAS Ctlgrs267608548
Max Magnitude0
ClinVar
Risk rs267608548(;)
Alt rs267608548(;)
Reference rs267608548(C;C)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296373delG
CLNSRC
CLNACC RCV000133283.2,