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rs61755761

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61755761(-;-)
Make rs61755761(-;C)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154032239
GeneMECP2
is asnp
is mentioned by
dbSNPrs61755761
ebirs61755761
HLIrs61755761
Exacrs61755761
Varsomers61755761
Maprs61755761
PheGenIrs61755761
hapmaprs61755761
1000 genomesrs61755761
hgdprs61755761
ensemblrs61755761
gopubmedrs61755761
geneviewrs61755761
scholarrs61755761
googlers61755761
pharmgkbrs61755761
gwascentralrs61755761
openSNPrs61755761
23andMers61755761
23andMe allrs61755761
SNP Nexus

SNPshotrs61755761
SNPdbers61755761
MSV3drs61755761
GWAS Ctlgrs61755761
Max Magnitude0
ClinVar
Risk rs61755761(;)
Alt rs61755761(;)
Reference rs61755761(C;C)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153297690delG
CLNSRC
CLNACC RCV000133075.2,