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rs61750238

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs61750238(A;T)
Make rs61750238(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031029
GeneMECP2
is asnp
is mentioned by
dbSNPrs61750238
ebirs61750238
HLIrs61750238
Exacrs61750238
Varsomers61750238
Maprs61750238
PheGenIrs61750238
hapmaprs61750238
1000 genomesrs61750238
hgdprs61750238
ensemblrs61750238
gopubmedrs61750238
geneviewrs61750238
scholarrs61750238
googlers61750238
pharmgkbrs61750238
gwascentralrs61750238
openSNPrs61750238
23andMers61750238
23andMe allrs61750238
SNP Nexus

SNPshotrs61750238
SNPdbers61750238
MSV3drs61750238
GWAS Ctlgrs61750238
Max Magnitude0
ClinVar
Risk rs61750238(T;T)
Alt rs61750238(T;T)
Reference rs61750238(A;A)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296480T>A
CLNSRC
CLNACC RCV000133240.2,