ClinVar Miner

List of variants in gene combination CAD, LOC126806171 reported as likely benign for Developmental and epileptic encephalopathy, 50

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_004341.5(CAD):c.2646-7A>G	rs202227357	0.00051
NM_004341.5(CAD):c.2576C>T (p.Pro859Leu)	rs144292695	0.00038

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