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rs61749717

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs61749717(A;T)
Make rs61749717(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031236
GeneMECP2
is asnp
is mentioned by
dbSNPrs61749717
ebirs61749717
HLIrs61749717
Exacrs61749717
Varsomers61749717
Maprs61749717
PheGenIrs61749717
hapmaprs61749717
1000 genomesrs61749717
hgdprs61749717
ensemblrs61749717
gopubmedrs61749717
geneviewrs61749717
scholarrs61749717
googlers61749717
pharmgkbrs61749717
gwascentralrs61749717
openSNPrs61749717
23andMers61749717
23andMe allrs61749717
SNP Nexus

SNPshotrs61749717
SNPdbers61749717
MSV3drs61749717
GWAS Ctlgrs61749717
Max Magnitude0
ClinVar
Risk rs61749717(C,T;C,T)
Alt rs61749717(C,T;C,T)
Reference rs61749717(A;A)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296687T>A
CLNSRC
CLNACC RCV000133169.2,