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rs61748428

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs61748428(A;T)
Make rs61748428(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031305
GeneMECP2
is asnp
is mentioned by
dbSNPrs61748428
ebirs61748428
HLIrs61748428
Exacrs61748428
Varsomers61748428
Maprs61748428
PheGenIrs61748428
hapmaprs61748428
1000 genomesrs61748428
hgdprs61748428
ensemblrs61748428
gopubmedrs61748428
geneviewrs61748428
scholarrs61748428
googlers61748428
pharmgkbrs61748428
gwascentralrs61748428
openSNPrs61748428
23andMers61748428
23andMe allrs61748428
SNP Nexus

SNPshotrs61748428
SNPdbers61748428
MSV3drs61748428
GWAS Ctlgrs61748428
Max Magnitude0
ClinVar
Risk rs61748428(T;T)
Alt rs61748428(T;T)
Reference rs61748428(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene MECP2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153296756T>A
CLNSRC
CLNACC RCV000133150.2,