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

rs61750242

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AGCCGGG;AGCCGGG) 0 common in clinvar
Make rs61750242(-;-)
Make rs61750242(-;AGCCGGG)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031010
GeneMECP2
is asnp
is mentioned by
dbSNPrs61750242
ebirs61750242
HLIrs61750242
Exacrs61750242
Varsomers61750242
Maprs61750242
PheGenIrs61750242
hapmaprs61750242
1000 genomesrs61750242
hgdprs61750242
ensemblrs61750242
gopubmedrs61750242
geneviewrs61750242
scholarrs61750242
googlers61750242
pharmgkbrs61750242
gwascentralrs61750242
openSNPrs61750242
23andMers61750242
23andMe allrs61750242
SNP Nexus

SNPshotrs61750242
SNPdbers61750242
MSV3drs61750242
GWAS Ctlgrs61750242
Max Magnitude0
ClinVar
Risk rs61750242(;)
Alt rs61750242(;)
Reference rs61750242(AGCCGGG;AGCCGGG)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296461_153296467delCCCGGCT
CLNSRC
CLNACC RCV000133245.2,