ClinVar Miner

List of variants in gene combination CLN5, FBXL3 reported as likely benign for adolescent-onset epilepsy syndrome

Included ClinVar conditions (80):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
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NM_006493.2(CLN5):c.789A>T (p.Val263=) rs751496223
NM_006493.2(CLN5):c.801A>C (p.Pro267=) rs752406072
NM_006493.3(CLN5):c.579C>A (p.Asn193Lys) rs138611001

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