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rs61753011

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs61753011(-;-)
Make rs61753011(-;T)
Make rs61753011(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030633
GeneMECP2
is asnp
is mentioned by
dbSNPrs61753011
ebirs61753011
HLIrs61753011
Exacrs61753011
Varsomers61753011
Maprs61753011
PheGenIrs61753011
hapmaprs61753011
1000 genomesrs61753011
hgdprs61753011
ensemblrs61753011
gopubmedrs61753011
geneviewrs61753011
scholarrs61753011
googlers61753011
pharmgkbrs61753011
gwascentralrs61753011
openSNPrs61753011
23andMers61753011
23andMe allrs61753011
SNP Nexus

SNPshotrs61753011
SNPdbers61753011
MSV3drs61753011
GWAS Ctlgrs61753011
Max Magnitude0
ClinVar
Risk rs61753011(T;T)
Alt rs61753011(T;T)
Reference rs61753011(;)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296084_153296085insA
CLNSRC
CLNACC RCV000132955.2,