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rs1064793576

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
ChromosomeX
Position154031138
GeneMECP2
is asnp
is mentioned by
dbSNPrs1064793576
dbSNP (classic)rs1064793576
ClinGenrs1064793576
ebirs1064793576
HLIrs1064793576
Exacrs1064793576
Gnomadrs1064793576
Varsomers1064793576
LitVarrs1064793576
Maprs1064793576
PheGenIrs1064793576
Biobankrs1064793576
1000 genomesrs1064793576
hgdprs1064793576
ensemblrs1064793576
geneviewrs1064793576
scholarrs1064793576
googlers1064793576
pharmgkbrs1064793576
gwascentralrs1064793576
openSNPrs1064793576
23andMers1064793576
SNPshotrs1064793576
SNPdbers1064793576
MSV3drs1064793576
GWAS Ctlgrs1064793576
Max Magnitude0
ClinVar
Risk rs1064793576(-;-)
Alt rs1064793576(-;-)
Reference Rs1064793576(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene MECP2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153296589delT
CLNSRC
CLNACC RCV000482709.1,