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rs267608445

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267608445(G;T)
Make rs267608445(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154032310
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608445
ebirs267608445
HLIrs267608445
Exacrs267608445
Varsomers267608445
Maprs267608445
PheGenIrs267608445
hapmaprs267608445
1000 genomesrs267608445
hgdprs267608445
ensemblrs267608445
gopubmedrs267608445
geneviewrs267608445
scholarrs267608445
googlers267608445
pharmgkbrs267608445
gwascentralrs267608445
openSNPrs267608445
23andMers267608445
23andMe allrs267608445
SNP Nexus

SNPshotrs267608445
SNPdbers267608445
MSV3drs267608445
GWAS Ctlgrs267608445
Max Magnitude0
ClinVar
Risk rs267608445(T;T)
Alt rs267608445(T;T)
Reference rs267608445(G;G)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153297761C>A
CLNSRC
CLNACC RCV000133043.2,