Have questions? Visit https://www.reddit.com/r/SNPedia

rs61749727

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61749727(-;-)
Make rs61749727(-;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031211
GeneMECP2
is asnp
is mentioned by
dbSNPrs61749727
ebirs61749727
HLIrs61749727
Exacrs61749727
Varsomers61749727
Maprs61749727
PheGenIrs61749727
hapmaprs61749727
1000 genomesrs61749727
hgdprs61749727
ensemblrs61749727
gopubmedrs61749727
geneviewrs61749727
scholarrs61749727
googlers61749727
pharmgkbrs61749727
gwascentralrs61749727
openSNPrs61749727
23andMers61749727
23andMe allrs61749727
SNP Nexus

SNPshotrs61749727
SNPdbers61749727
MSV3drs61749727
GWAS Ctlgrs61749727
Max Magnitude0
ClinVar
Risk rs61749727(;)
Alt rs61749727(;)
Reference rs61749727(G;G)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296662delC
CLNSRC
CLNACC RCV000133179.2,