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rs61748398

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
(-;-) 0 common/normal
Make rs61748398(-;T)
Make rs61748398(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031399
GeneMECP2
is asnp
is mentioned by
dbSNPrs61748398
ebirs61748398
HLIrs61748398
Exacrs61748398
Varsomers61748398
Maprs61748398
PheGenIrs61748398
hapmaprs61748398
1000 genomesrs61748398
hgdprs61748398
ensemblrs61748398
gopubmedrs61748398
geneviewrs61748398
scholarrs61748398
googlers61748398
pharmgkbrs61748398
gwascentralrs61748398
openSNPrs61748398
23andMers61748398
23andMe allrs61748398
SNP Nexus

SNPshotrs61748398
SNPdbers61748398
MSV3drs61748398
GWAS Ctlgrs61748398
Max Magnitude0
ClinVar
Risk rs61748398(T;T)
Alt rs61748398(T;T)
Reference rs61748398(;)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296850_153296851insA
CLNSRC
CLNACC RCV000133107.2,