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rs1064797047

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
ChromosomeX
Position154032331
GeneMECP2
is asnp
is mentioned by
dbSNPrs1064797047
dbSNP (old)rs1064797047
ClinGenrs1064797047
ebirs1064797047
HLIrs1064797047
Exacrs1064797047
Gnomadrs1064797047
Varsomers1064797047
Maprs1064797047
PheGenIrs1064797047
Biobankrs1064797047
1000 genomesrs1064797047
hgdprs1064797047
ensemblrs1064797047
gopubmedrs1064797047
geneviewrs1064797047
scholarrs1064797047
googlers1064797047
pharmgkbrs1064797047
gwascentralrs1064797047
openSNPrs1064797047
23andMers1064797047
23andMe allrs1064797047
SNPshotrs1064797047
SNPdbers1064797047
MSV3drs1064797047
GWAS Ctlgrs1064797047
Max Magnitude0
ClinVar
Risk rs1064797047(T;T)
Alt rs1064797047(T;T)
Reference Rs1064797047(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MECP2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153297782G>A
CLNSRC
CLNACC RCV000487257.1,