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

rs267608425

From SNPedia

Orientationminus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs267608425(-;-)
Make rs267608425(-;AA)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154032476
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608425
ebirs267608425
HLIrs267608425
Exacrs267608425
Varsomers267608425
Maprs267608425
PheGenIrs267608425
hapmaprs267608425
1000 genomesrs267608425
hgdprs267608425
ensemblrs267608425
gopubmedrs267608425
geneviewrs267608425
scholarrs267608425
googlers267608425
pharmgkbrs267608425
gwascentralrs267608425
openSNPrs267608425
23andMers267608425
23andMe allrs267608425
SNP Nexus

SNPshotrs267608425
SNPdbers267608425
MSV3drs267608425
GWAS Ctlgrs267608425
Max Magnitude0
ClinVar
Risk rs267608425(;)
Alt rs267608425(;)
Reference rs267608425(AA;AA)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153297927_153297928delTT
CLNSRC
CLNACC RCV000132848.2,