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rs61748420

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61748420(C;T)
Make rs61748420(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position154031329
GeneMECP2
is asnp
is mentioned by
dbSNPrs61748420
ebirs61748420
HLIrs61748420
Exacrs61748420
Varsomers61748420
Maprs61748420
PheGenIrs61748420
hapmaprs61748420
1000 genomesrs61748420
hgdprs61748420
ensemblrs61748420
gopubmedrs61748420
geneviewrs61748420
scholarrs61748420
googlers61748420
pharmgkbrs61748420
gwascentralrs61748420
openSNPrs61748420
23andMers61748420
23andMe allrs61748420
SNP Nexus

SNPshotrs61748420
SNPdbers61748420
MSV3drs61748420
GWAS Ctlgrs61748420
Max Magnitude0
ClinVar
Risk rs61748420(T;T)
Alt rs61748420(T;T)
Reference rs61748420(C;C)
Significance Pathogenic
Disease Mental retardation Rett syndrome
Variation info
Gene MECP2
CLNDBN Mental retardation, X-linked, syndromic 13 Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296780G>A
CLNSRC
CLNACC RCV000133142.2, RCV000193537.1,