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rs61748399

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs61748399(A;T)
Make rs61748399(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031398
GeneMECP2
is asnp
is mentioned by
dbSNPrs61748399
ebirs61748399
HLIrs61748399
Exacrs61748399
Varsomers61748399
Maprs61748399
PheGenIrs61748399
hapmaprs61748399
1000 genomesrs61748399
hgdprs61748399
ensemblrs61748399
gopubmedrs61748399
geneviewrs61748399
scholarrs61748399
googlers61748399
pharmgkbrs61748399
gwascentralrs61748399
openSNPrs61748399
23andMers61748399
23andMe allrs61748399
SNP Nexus

SNPshotrs61748399
SNPdbers61748399
MSV3drs61748399
GWAS Ctlgrs61748399
Max Magnitude0
ClinVar
Risk rs61748399(T;T)
Alt rs61748399(T;T)
Reference rs61748399(A;A)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296849T>A
CLNSRC
CLNACC RCV000133108.2,