ClinVar Miner

List of variants reported as likely pathogenic for X-linked epilepsy-learning disabilities-behavior disorders syndrome

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 3
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HGVS dbSNP
NM_006950.3(SYN1):c.1297C>T (p.His433Tyr) rs41298474
NM_006950.3(SYN1):c.1439dup (p.Leu481fs) rs1556857481
NM_006950.3(SYN1):c.528-2A>T rs1556860663

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