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rs267608538

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267608538(-;-)
Make rs267608538(-;A)
Make rs267608538(A;A)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030958
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608538
ebirs267608538
HLIrs267608538
Exacrs267608538
Varsomers267608538
Maprs267608538
PheGenIrs267608538
hapmaprs267608538
1000 genomesrs267608538
hgdprs267608538
ensemblrs267608538
gopubmedrs267608538
geneviewrs267608538
scholarrs267608538
googlers267608538
pharmgkbrs267608538
gwascentralrs267608538
openSNPrs267608538
23andMers267608538
23andMe allrs267608538
SNP Nexus

SNPshotrs267608538
SNPdbers267608538
MSV3drs267608538
GWAS Ctlgrs267608538
Max Magnitude0
ClinVar
Risk rs267608538(A;A)
Alt rs267608538(A;A)
Reference rs267608538(;)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296410dupT
CLNSRC
CLNACC RCV000133262.2,