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rs61750232

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs61750232(-;-)
Make rs61750232(-;G)
Make rs61750232(G;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031072
GeneMECP2
is asnp
is mentioned by
dbSNPrs61750232
ebirs61750232
HLIrs61750232
Exacrs61750232
Varsomers61750232
Maprs61750232
PheGenIrs61750232
hapmaprs61750232
1000 genomesrs61750232
hgdprs61750232
ensemblrs61750232
gopubmedrs61750232
geneviewrs61750232
scholarrs61750232
googlers61750232
pharmgkbrs61750232
gwascentralrs61750232
openSNPrs61750232
23andMers61750232
23andMe allrs61750232
SNP Nexus

SNPshotrs61750232
SNPdbers61750232
MSV3drs61750232
GWAS Ctlgrs61750232
Max Magnitude0
ClinVar
Risk rs61750232(G;G)
Alt rs61750232(G;G)
Reference rs61750232(;)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296524dupC
CLNSRC
CLNACC RCV000133231.2,