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rs797045292

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797045292(-;C)
Make rs797045292(C;C)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position25004887
GeneARX
is asnp
is mentioned by
dbSNPrs797045292
dbSNP (old)rs797045292
ClinGenrs797045292
ebirs797045292
HLIrs797045292
Exacrs797045292
Varsomers797045292
Maprs797045292
PheGenIrs797045292
Biobankrs797045292
1000 genomesrs797045292
hgdprs797045292
ensemblrs797045292
gopubmedrs797045292
geneviewrs797045292
scholarrs797045292
googlers797045292
pharmgkbrs797045292
gwascentralrs797045292
openSNPrs797045292
23andMers797045292
23andMe allrs797045292
SNP Nexus

SNPshotrs797045292
SNPdbers797045292
MSV3drs797045292
GWAS Ctlgrs797045292
Max Magnitude0
ClinVar
Risk rs797045292(C;C)
Alt rs797045292(C;C)
Reference Rs797045292(-;-)
Significance Pathogenic
Disease Lissencephaly 2
Variation info
Gene ARX
CLNDBN Lissencephaly 2, X-linked
Reversed 1
HGVS NC_000023.10:g.25023005dupG
CLNSRC
CLNACC RCV000195080.1,