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rs267608536

From SNPedia

Orientationminus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs267608536(-;-)
Make rs267608536(-;AA)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030962
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608536
ebirs267608536
HLIrs267608536
Exacrs267608536
Varsomers267608536
Maprs267608536
PheGenIrs267608536
hapmaprs267608536
1000 genomesrs267608536
hgdprs267608536
ensemblrs267608536
gopubmedrs267608536
geneviewrs267608536
scholarrs267608536
googlers267608536
pharmgkbrs267608536
gwascentralrs267608536
openSNPrs267608536
23andMers267608536
23andMe allrs267608536
SNP Nexus

SNPshotrs267608536
SNPdbers267608536
MSV3drs267608536
GWAS Ctlgrs267608536
Max Magnitude0
ClinVar
Risk rs267608536(;)
Alt rs267608536(;)
Reference rs267608536(AA;AA)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296413_153296414delTT
CLNSRC
CLNACC RCV000133261.2,