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rs398124506

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GC;GC) 0 common in clinvar
Make rs398124506(-;-)
Make rs398124506(-;GC)
ReferenceGRCh38 38.1/141
ChromosomeX
Position25007407
GeneARX
is asnp
is mentioned by
dbSNPrs398124506
ebirs398124506
HLIrs398124506
Exacrs398124506
Varsomers398124506
Maprs398124506
PheGenIrs398124506
hapmaprs398124506
1000 genomesrs398124506
hgdprs398124506
ensemblrs398124506
gopubmedrs398124506
geneviewrs398124506
scholarrs398124506
googlers398124506
pharmgkbrs398124506
gwascentralrs398124506
openSNPrs398124506
23andMers398124506
23andMe allrs398124506
SNP Nexus

SNPshotrs398124506
SNPdbers398124506
MSV3drs398124506
GWAS Ctlgrs398124506
Max Magnitude0
ClinVar
Risk rs398124506(;)
Alt rs398124506(;)
Reference rs398124506(GC;GC)
Significance Pathogenic
Disease not provided
Variation info
Gene ARX
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.25025524_25025525delGC
CLNSRC ClinVar
CLNACC RCV000082598.4,