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rs797045298

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797045298(-;G)
Make rs797045298(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position25013585
GeneARX
is asnp
is mentioned by
dbSNPrs797045298
dbSNP (old)rs797045298
ClinGenrs797045298
ebirs797045298
HLIrs797045298
Exacrs797045298
Gnomadrs797045298
Varsomers797045298
Maprs797045298
PheGenIrs797045298
Biobankrs797045298
1000 genomesrs797045298
hgdprs797045298
ensemblrs797045298
gopubmedrs797045298
geneviewrs797045298
scholarrs797045298
googlers797045298
pharmgkbrs797045298
gwascentralrs797045298
openSNPrs797045298
23andMers797045298
23andMe allrs797045298
SNP Nexus

SNPshotrs797045298
SNPdbers797045298
MSV3drs797045298
GWAS Ctlgrs797045298
Max Magnitude0
ClinVar
Risk rs797045298(G;G)
Alt rs797045298(G;G)
Reference Rs797045298(-;-)
Significance Pathogenic
Disease Lissencephaly 2
Variation info
Gene ARX
CLNDBN Lissencephaly 2, X-linked
Reversed 1
HGVS NC_000023.10:g.25031703dupC
CLNSRC
CLNACC RCV000192991.1,