ClinVar Miner

List of variants in gene combination ARX, LOC109610631 reported as likely pathogenic for ARX-related epileptic encephalopathy

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 1
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HGVS dbSNP
NM_139058.3(ARX):c.426_461dup (p.Gly143_Ala154dup) rs1556056131

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