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rs267608525

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267608525(C;T)
Make rs267608525(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031044
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608525
ebirs267608525
HLIrs267608525
Exacrs267608525
Varsomers267608525
Maprs267608525
PheGenIrs267608525
hapmaprs267608525
1000 genomesrs267608525
hgdprs267608525
ensemblrs267608525
gopubmedrs267608525
geneviewrs267608525
scholarrs267608525
googlers267608525
pharmgkbrs267608525
gwascentralrs267608525
openSNPrs267608525
23andMers267608525
23andMe allrs267608525
SNP Nexus

SNPshotrs267608525
SNPdbers267608525
MSV3drs267608525
GWAS Ctlgrs267608525
Max Magnitude0
ClinVar
Risk rs267608525(T;T)
Alt rs267608525(T;T)
Reference rs267608525(C;C)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296495G>A
CLNSRC Quest Diagnostics
CLNACC RCV000133237.3,