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rs1064796837

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
ChromosomeX
Position154030619
GeneMECP2
is asnp
is mentioned by
dbSNPrs1064796837
dbSNP (old)rs1064796837
ClinGenrs1064796837
ebirs1064796837
HLIrs1064796837
Exacrs1064796837
Gnomadrs1064796837
Varsomers1064796837
Maprs1064796837
PheGenIrs1064796837
Biobankrs1064796837
1000 genomesrs1064796837
hgdprs1064796837
ensemblrs1064796837
gopubmedrs1064796837
geneviewrs1064796837
scholarrs1064796837
googlers1064796837
pharmgkbrs1064796837
gwascentralrs1064796837
openSNPrs1064796837
23andMers1064796837
23andMe allrs1064796837
SNPshotrs1064796837
SNPdbers1064796837
MSV3drs1064796837
GWAS Ctlgrs1064796837
Max Magnitude0
ClinVar
Risk rs1064796837(-;-)
Alt rs1064796837(-;-)
Reference Rs1064796837(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MECP2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153296070delA
CLNSRC
CLNACC RCV000480265.1,