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rs1064794843

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
ChromosomeX
Position25004747
GeneARX
is asnp
is mentioned by
dbSNPrs1064794843
dbSNP (old)rs1064794843
ClinGenrs1064794843
ebirs1064794843
HLIrs1064794843
Exacrs1064794843
Gnomadrs1064794843
Varsomers1064794843
LitVarrs1064794843
Maprs1064794843
PheGenIrs1064794843
Biobankrs1064794843
1000 genomesrs1064794843
hgdprs1064794843
ensemblrs1064794843
gopubmedrs1064794843
geneviewrs1064794843
scholarrs1064794843
googlers1064794843
pharmgkbrs1064794843
gwascentralrs1064794843
openSNPrs1064794843
23andMers1064794843
23andMe allrs1064794843
SNPshotrs1064794843
SNPdbers1064794843
MSV3drs1064794843
GWAS Ctlgrs1064794843
Max Magnitude0
ClinVar
Risk rs1064794843(G;G)
Alt rs1064794843(G;G)
Reference Rs1064794843(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ARX
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.25022864T>C
CLNSRC
CLNACC RCV000485667.1,