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rs61753979

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61753979(C;T)
Make rs61753979(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030471
GeneMECP2
is asnp
is mentioned by
dbSNPrs61753979
ebirs61753979
HLIrs61753979
Exacrs61753979
Varsomers61753979
Maprs61753979
PheGenIrs61753979
hapmaprs61753979
1000 genomesrs61753979
hgdprs61753979
ensemblrs61753979
gopubmedrs61753979
geneviewrs61753979
scholarrs61753979
googlers61753979
pharmgkbrs61753979
gwascentralrs61753979
openSNPrs61753979
23andMers61753979
23andMe allrs61753979
SNP Nexus

SNPshotrs61753979
SNPdbers61753979
MSV3drs61753979
GWAS Ctlgrs61753979
Max Magnitude0
ClinVar
Risk rs61753979(T;T)
Alt rs61753979(T;T)
Reference rs61753979(C;C)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153295922G>A
CLNSRC
CLNACC RCV000132995.3,