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rs797045303

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GC;GC) 0 common in clinvar
Make rs797045303(GC;TA)
Make rs797045303(TA;TA)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position25013432
GeneARX
is asnp
is mentioned by
dbSNPrs797045303
dbSNP (old)rs797045303
ClinGenrs797045303
ebirs797045303
HLIrs797045303
Exacrs797045303
Gnomadrs797045303
Varsomers797045303
Maprs797045303
PheGenIrs797045303
Biobankrs797045303
1000 genomesrs797045303
hgdprs797045303
ensemblrs797045303
gopubmedrs797045303
geneviewrs797045303
scholarrs797045303
googlers797045303
pharmgkbrs797045303
gwascentralrs797045303
openSNPrs797045303
23andMers797045303
23andMe allrs797045303
SNP Nexus

SNPshotrs797045303
SNPdbers797045303
MSV3drs797045303
GWAS Ctlgrs797045303
Max Magnitude0
ClinVar
Risk rs797045303(TA;TA)
Alt rs797045303(TA;TA)
Reference Rs797045303(GC;GC)
Significance Pathogenic
Disease Lissencephaly 2
Variation info
Gene ARX
CLNDBN Lissencephaly 2, X-linked
Reversed 1
HGVS NC_000023.10:g.25031549_25031550delGCinsTA
CLNSRC
CLNACC RCV000192847.1,