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

rs61752375

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs61752375(A;T)
Make rs61752375(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030741
GeneMECP2
is asnp
is mentioned by
dbSNPrs61752375
ebirs61752375
HLIrs61752375
Exacrs61752375
Varsomers61752375
Maprs61752375
PheGenIrs61752375
hapmaprs61752375
1000 genomesrs61752375
hgdprs61752375
ensemblrs61752375
gopubmedrs61752375
geneviewrs61752375
scholarrs61752375
googlers61752375
pharmgkbrs61752375
gwascentralrs61752375
openSNPrs61752375
23andMers61752375
23andMe allrs61752375
SNP Nexus

SNPshotrs61752375
SNPdbers61752375
MSV3drs61752375
GWAS Ctlgrs61752375
Max Magnitude0
ClinVar
Risk rs61752375(T;T)
Alt rs61752375(T;T)
Reference rs61752375(A;A)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296192T>A
CLNSRC
CLNACC RCV000132851.2,