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rs61749718

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs61749718(A;T)
Make rs61749718(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031230
GeneMECP2
is asnp
is mentioned by
dbSNPrs61749718
ebirs61749718
HLIrs61749718
Exacrs61749718
Varsomers61749718
Maprs61749718
PheGenIrs61749718
hapmaprs61749718
1000 genomesrs61749718
hgdprs61749718
ensemblrs61749718
gopubmedrs61749718
geneviewrs61749718
scholarrs61749718
googlers61749718
pharmgkbrs61749718
gwascentralrs61749718
openSNPrs61749718
23andMers61749718
23andMe allrs61749718
SNP Nexus

SNPshotrs61749718
SNPdbers61749718
MSV3drs61749718
GWAS Ctlgrs61749718
Max Magnitude0
ClinVar
Risk rs61749718(T;T)
Alt rs61749718(T;T)
Reference rs61749718(A;A)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296681T>A
CLNSRC
CLNACC RCV000133171.2,