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rs61748402

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61748402(-;-)
Make rs61748402(-;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031377
GeneMECP2
is asnp
is mentioned by
dbSNPrs61748402
ebirs61748402
HLIrs61748402
Exacrs61748402
Varsomers61748402
Maprs61748402
PheGenIrs61748402
hapmaprs61748402
1000 genomesrs61748402
hgdprs61748402
ensemblrs61748402
gopubmedrs61748402
geneviewrs61748402
scholarrs61748402
googlers61748402
pharmgkbrs61748402
gwascentralrs61748402
openSNPrs61748402
23andMers61748402
23andMe allrs61748402
SNP Nexus

SNPshotrs61748402
SNPdbers61748402
MSV3drs61748402
GWAS Ctlgrs61748402
Max Magnitude0
ClinVar
Risk rs61748402(;)
Alt rs61748402(;)
Reference rs61748402(G;G)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296828delC
CLNSRC
CLNACC RCV000133113.2,