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rs61754428

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GATA;GATA) 0 common in clinvar
Make rs61754428(-;-)
Make rs61754428(-;GATA)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154032481
GeneMECP2
is asnp
is mentioned by
dbSNPrs61754428
ebirs61754428
HLIrs61754428
Exacrs61754428
Varsomers61754428
Maprs61754428
PheGenIrs61754428
hapmaprs61754428
1000 genomesrs61754428
hgdprs61754428
ensemblrs61754428
gopubmedrs61754428
geneviewrs61754428
scholarrs61754428
googlers61754428
pharmgkbrs61754428
gwascentralrs61754428
openSNPrs61754428
23andMers61754428
23andMe allrs61754428
SNP Nexus

SNPshotrs61754428
SNPdbers61754428
MSV3drs61754428
GWAS Ctlgrs61754428
Max Magnitude0
ClinVar
Risk rs61754428(;)
Alt rs61754428(;)
Reference rs61754428(GATA;GATA)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153297932_153297935delTATC
CLNSRC
CLNACC RCV000132828.2,