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rs267608495

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267608495(A;T)
Make rs267608495(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031290
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608495
ebirs267608495
HLIrs267608495
Exacrs267608495
Varsomers267608495
Maprs267608495
PheGenIrs267608495
hapmaprs267608495
1000 genomesrs267608495
hgdprs267608495
ensemblrs267608495
gopubmedrs267608495
geneviewrs267608495
scholarrs267608495
googlers267608495
pharmgkbrs267608495
gwascentralrs267608495
openSNPrs267608495
23andMers267608495
23andMe allrs267608495
SNP Nexus

SNPshotrs267608495
SNPdbers267608495
MSV3drs267608495
GWAS Ctlgrs267608495
Max Magnitude0
ClinVar
Risk rs267608495(T;T)
Alt rs267608495(T;T)
Reference rs267608495(A;A)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296741T>A
CLNSRC
CLNACC RCV000133155.2,