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rs267608510

From SNPedia

Orientationminus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs267608510(-;-)
Make rs267608510(-;TG)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031176
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608510
ebirs267608510
HLIrs267608510
Exacrs267608510
Varsomers267608510
Maprs267608510
PheGenIrs267608510
hapmaprs267608510
1000 genomesrs267608510
hgdprs267608510
ensemblrs267608510
gopubmedrs267608510
geneviewrs267608510
scholarrs267608510
googlers267608510
pharmgkbrs267608510
gwascentralrs267608510
openSNPrs267608510
23andMers267608510
23andMe allrs267608510
SNP Nexus

SNPshotrs267608510
SNPdbers267608510
MSV3drs267608510
GWAS Ctlgrs267608510
Max Magnitude0
ClinVar
Risk rs267608510(;)
Alt rs267608510(;)
Reference rs267608510(TG;TG)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296627_153296628delCA
CLNSRC
CLNACC RCV000133188.2,