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rs398124520

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AACA;AACA) 0 common in clinvar
Make rs398124520(-;-)
Make rs398124520(-;AACA)
ReferenceGRCh38 38.1/141
ChromosomeX
Position25013012
GeneARX
is asnp
is mentioned by
dbSNPrs398124520
ebirs398124520
HLIrs398124520
Exacrs398124520
Varsomers398124520
Maprs398124520
PheGenIrs398124520
hapmaprs398124520
1000 genomesrs398124520
hgdprs398124520
ensemblrs398124520
gopubmedrs398124520
geneviewrs398124520
scholarrs398124520
googlers398124520
pharmgkbrs398124520
gwascentralrs398124520
openSNPrs398124520
23andMers398124520
23andMe allrs398124520
SNP Nexus

SNPshotrs398124520
SNPdbers398124520
MSV3drs398124520
GWAS Ctlgrs398124520
Max Magnitude0
ClinVar
Risk rs398124520(;)
Alt rs398124520(;)
Reference rs398124520(AACA;AACA)
Significance Pathogenic
Disease not provided
Variation info
Gene ARX
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.25031129_25031132delTGTT
CLNSRC HGMD
CLNACC RCV000082614.3,