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rs398122854

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398122854(C;G)
Make rs398122854(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position25015657
GeneARX
is asnp
is mentioned by
dbSNPrs398122854
ebirs398122854
HLIrs398122854
Exacrs398122854
Varsomers398122854
Maprs398122854
PheGenIrs398122854
hapmaprs398122854
1000 genomesrs398122854
hgdprs398122854
ensemblrs398122854
gopubmedrs398122854
geneviewrs398122854
scholarrs398122854
googlers398122854
pharmgkbrs398122854
gwascentralrs398122854
openSNPrs398122854
23andMers398122854
23andMe allrs398122854
SNP Nexus

SNPshotrs398122854
SNPdbers398122854
MSV3drs398122854
GWAS Ctlgrs398122854
Max Magnitude0
ClinVar
Risk rs398122854(G;G)
Alt rs398122854(G;G)
Reference rs398122854(C;C)
Significance Pathogenic
Disease Epileptic encephalopathy
Variation info
Gene ARX
CLNDBN Epileptic encephalopathy, early infantile, 1
Reversed 1
HGVS NC_000023.10:g.25033774G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000022856.8,