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

rs267608446

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267608446(-;-)
Make rs267608446(-;G)
Make rs267608446(G;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154032308
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608446
ebirs267608446
HLIrs267608446
Exacrs267608446
Varsomers267608446
Maprs267608446
PheGenIrs267608446
hapmaprs267608446
1000 genomesrs267608446
hgdprs267608446
ensemblrs267608446
gopubmedrs267608446
geneviewrs267608446
scholarrs267608446
googlers267608446
pharmgkbrs267608446
gwascentralrs267608446
openSNPrs267608446
23andMers267608446
23andMe allrs267608446
SNP Nexus

SNPshotrs267608446
SNPdbers267608446
MSV3drs267608446
GWAS Ctlgrs267608446
Max Magnitude0
ClinVar
Risk rs267608446(G;G)
Alt rs267608446(G;G)
Reference rs267608446(;)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153297760dupC
CLNSRC
CLNACC RCV000133044.2,