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rs61748425

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61748425(C;T)
Make rs61748425(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031320
GeneMECP2
is asnp
is mentioned by
dbSNPrs61748425
ebirs61748425
HLIrs61748425
Exacrs61748425
Varsomers61748425
Maprs61748425
PheGenIrs61748425
hapmaprs61748425
1000 genomesrs61748425
hgdprs61748425
ensemblrs61748425
gopubmedrs61748425
geneviewrs61748425
scholarrs61748425
googlers61748425
pharmgkbrs61748425
gwascentralrs61748425
openSNPrs61748425
23andMers61748425
23andMe allrs61748425
SNP Nexus

SNPshotrs61748425
SNPdbers61748425
MSV3drs61748425
GWAS Ctlgrs61748425
Max Magnitude0
ClinVar
Risk rs61748425(T;T)
Alt rs61748425(T;T)
Reference rs61748425(C;C)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296771G>A
CLNSRC
CLNACC RCV000133144.2,