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rs61754453

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61754453(C;G)
Make rs61754453(G;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154032282
GeneMECP2
is asnp
is mentioned by
dbSNPrs61754453
ebirs61754453
HLIrs61754453
Exacrs61754453
Varsomers61754453
Maprs61754453
PheGenIrs61754453
hapmaprs61754453
1000 genomesrs61754453
hgdprs61754453
ensemblrs61754453
gopubmedrs61754453
geneviewrs61754453
scholarrs61754453
googlers61754453
pharmgkbrs61754453
gwascentralrs61754453
openSNPrs61754453
23andMers61754453
23andMe allrs61754453
SNP Nexus

SNPshotrs61754453
SNPdbers61754453
MSV3drs61754453
GWAS Ctlgrs61754453
Max Magnitude0
ClinVar
Risk rs61754453(A,G,T;A,G,T)
Alt rs61754453(A,G,T;A,G,T)
Reference rs61754453(C;C)
Significance Other
Disease Rett syndrome Angelman syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome Angelman syndrome
Reversed 1
HGVS NC_000023.10:g.153297733G>A; NC_000023.10:g.153297733G>C; NC_000023.10:g.153297733G>T
CLNSRC
CLNACC RCV000133059.2, RCV000133058.2, RCV000170238.2, RCV000133057.2,