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rs63259763

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs63259763(A;T)
Make rs63259763(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031068
GeneMECP2
is asnp
is mentioned by
dbSNPrs63259763
ebirs63259763
HLIrs63259763
Exacrs63259763
Varsomers63259763
Maprs63259763
PheGenIrs63259763
hapmaprs63259763
1000 genomesrs63259763
hgdprs63259763
ensemblrs63259763
gopubmedrs63259763
geneviewrs63259763
scholarrs63259763
googlers63259763
pharmgkbrs63259763
gwascentralrs63259763
openSNPrs63259763
23andMers63259763
23andMe allrs63259763
SNP Nexus

SNPshotrs63259763
SNPdbers63259763
MSV3drs63259763
GWAS Ctlgrs63259763
Max Magnitude0
ClinVar
Risk rs63259763(T;T)
Alt rs63259763(T;T)
Reference rs63259763(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene MECP2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153296519T>A
CLNSRC
CLNACC RCV000133234.2,