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rs267608569

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267608569(C;G)
Make rs267608569(G;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030710
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608569
ebirs267608569
HLIrs267608569
Exacrs267608569
Varsomers267608569
Maprs267608569
PheGenIrs267608569
hapmaprs267608569
1000 genomesrs267608569
hgdprs267608569
ensemblrs267608569
gopubmedrs267608569
geneviewrs267608569
scholarrs267608569
googlers267608569
pharmgkbrs267608569
gwascentralrs267608569
openSNPrs267608569
23andMers267608569
23andMe allrs267608569
SNP Nexus

SNPshotrs267608569
SNPdbers267608569
MSV3drs267608569
GWAS Ctlgrs267608569
Max Magnitude0
ClinVar
Risk rs267608569(A,G;A,G)
Alt rs267608569(A,G;A,G)
Reference rs267608569(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.153296161G>C
CLNSRC
CLNACC RCV000132859.2, RCV000193072.1,