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

rs61750233

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61750233(-;-)
Make rs61750233(-;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031073
GeneMECP2
is asnp
is mentioned by
dbSNPrs61750233
ebirs61750233
HLIrs61750233
Exacrs61750233
Varsomers61750233
Maprs61750233
PheGenIrs61750233
hapmaprs61750233
1000 genomesrs61750233
hgdprs61750233
ensemblrs61750233
gopubmedrs61750233
geneviewrs61750233
scholarrs61750233
googlers61750233
pharmgkbrs61750233
gwascentralrs61750233
openSNPrs61750233
23andMers61750233
23andMe allrs61750233
SNP Nexus

SNPshotrs61750233
SNPdbers61750233
MSV3drs61750233
GWAS Ctlgrs61750233
Max Magnitude0
ClinVar
Risk rs61750233(;)
Alt rs61750233(;)
Reference rs61750233(G;G)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296524delC
CLNSRC
CLNACC RCV000133230.3,