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rs61752372

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61752372(A;A)
Make rs61752372(A;C)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030749
GeneMECP2
is asnp
is mentioned by
dbSNPrs61752372
ebirs61752372
HLIrs61752372
Exacrs61752372
Varsomers61752372
Maprs61752372
PheGenIrs61752372
hapmaprs61752372
1000 genomesrs61752372
hgdprs61752372
ensemblrs61752372
gopubmedrs61752372
geneviewrs61752372
scholarrs61752372
googlers61752372
pharmgkbrs61752372
gwascentralrs61752372
openSNPrs61752372
23andMers61752372
23andMe allrs61752372
SNP Nexus

SNPshotrs61752372
SNPdbers61752372
MSV3drs61752372
GWAS Ctlgrs61752372
Max Magnitude0
ClinVar
Risk rs61752372(A;A)
Alt rs61752372(A;A)
Reference rs61752372(C;C)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296200G>T
CLNSRC
CLNACC RCV000132847.2,