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rs267608465

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267608465(C;G)
Make rs267608465(G;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031453
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608465
ebirs267608465
HLIrs267608465
Exacrs267608465
Varsomers267608465
Maprs267608465
PheGenIrs267608465
hapmaprs267608465
1000 genomesrs267608465
hgdprs267608465
ensemblrs267608465
gopubmedrs267608465
geneviewrs267608465
scholarrs267608465
googlers267608465
pharmgkbrs267608465
gwascentralrs267608465
openSNPrs267608465
23andMers267608465
23andMe allrs267608465
SNP Nexus

SNPshotrs267608465
SNPdbers267608465
MSV3drs267608465
GWAS Ctlgrs267608465
Max Magnitude0
ClinVar
Risk rs267608465(G,T;G,T)
Alt rs267608465(G,T;G,T)
Reference rs267608465(C;C)
Significance Pathogenic
Disease not provided Rett syndrome
Variation info
Gene MECP2
CLNDBN not provided Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296904G>C
CLNSRC
CLNACC RCV000144115.1, RCV000170202.1,