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rs61748415

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs61748415(-;-)
Make rs61748415(-;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031348
GeneMECP2
is asnp
is mentioned by
dbSNPrs61748415
ebirs61748415
HLIrs61748415
Exacrs61748415
Varsomers61748415
Maprs61748415
PheGenIrs61748415
hapmaprs61748415
1000 genomesrs61748415
hgdprs61748415
ensemblrs61748415
gopubmedrs61748415
geneviewrs61748415
scholarrs61748415
googlers61748415
pharmgkbrs61748415
gwascentralrs61748415
openSNPrs61748415
23andMers61748415
23andMe allrs61748415
SNP Nexus

SNPshotrs61748415
SNPdbers61748415
MSV3drs61748415
GWAS Ctlgrs61748415
Max Magnitude0
ClinVar
Risk rs61748415(;)
Alt rs61748415(;)
Reference rs61748415(T;T)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296799delA
CLNSRC
CLNACC RCV000133134.2,