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rs1064796513

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
ChromosomeX
Position154032208
GeneMECP2
is asnp
is mentioned by
dbSNPrs1064796513
dbSNP (classic)rs1064796513
ClinGenrs1064796513
ebirs1064796513
HLIrs1064796513
Exacrs1064796513
Gnomadrs1064796513
Varsomers1064796513
LitVarrs1064796513
Maprs1064796513
PheGenIrs1064796513
Biobankrs1064796513
1000 genomesrs1064796513
hgdprs1064796513
ensemblrs1064796513
geneviewrs1064796513
scholarrs1064796513
googlers1064796513
pharmgkbrs1064796513
gwascentralrs1064796513
openSNPrs1064796513
23andMers1064796513
23andMe allrs1064796513
SNPshotrs1064796513
SNPdbers1064796513
MSV3drs1064796513
GWAS Ctlgrs1064796513
Max Magnitude0
ClinVar
Risk rs1064796513(G;G)
Alt rs1064796513(G;G)
Reference Rs1064796513(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MECP2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153297659T>C
CLNSRC
CLNACC RCV000478123.1,