Have questions? Visit https://www.reddit.com/r/SNPedia

rs267608409

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267608409(A;A)
Make rs267608409(A;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154092182
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608409
ebirs267608409
HLIrs267608409
Exacrs267608409
Varsomers267608409
Maprs267608409
PheGenIrs267608409
hapmaprs267608409
1000 genomesrs267608409
hgdprs267608409
ensemblrs267608409
gopubmedrs267608409
geneviewrs267608409
scholarrs267608409
googlers267608409
pharmgkbrs267608409
gwascentralrs267608409
openSNPrs267608409
23andMers267608409
23andMe allrs267608409
SNP Nexus

SNPshotrs267608409
SNPdbers267608409
MSV3drs267608409
GWAS Ctlgrs267608409
Max Magnitude0
ClinVar
Risk rs267608409(A;A)
Alt rs267608409(A;A)
Reference rs267608409(T;T)
Significance Pathogenic
Disease not provided Rett syndrome
Variation info
Gene MECP2
CLNDBN not provided Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153357640A>T
CLNSRC
CLNACC RCV000144092.1, RCV000170166.1,