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rs61749726

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61749726(G;T)
Make rs61749726(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031215
GeneMECP2
is asnp
is mentioned by
dbSNPrs61749726
ebirs61749726
HLIrs61749726
Exacrs61749726
Varsomers61749726
Maprs61749726
PheGenIrs61749726
hapmaprs61749726
1000 genomesrs61749726
hgdprs61749726
ensemblrs61749726
gopubmedrs61749726
geneviewrs61749726
scholarrs61749726
googlers61749726
pharmgkbrs61749726
gwascentralrs61749726
openSNPrs61749726
23andMers61749726
23andMe allrs61749726
SNP Nexus

SNPshotrs61749726
SNPdbers61749726
MSV3drs61749726
GWAS Ctlgrs61749726
Max Magnitude0
ClinVar
Risk rs61749726(C,T;C,T)
Alt rs61749726(C,T;C,T)
Reference rs61749726(G;G)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296666C>A
CLNSRC
CLNACC RCV000133176.2,