ClinVar Miner

List of variants in gene combination HBA-LCR, NPRL3 reported as not provided for Epilepsy, familial focal, with variable foci 3

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_001077350.3(NPRL3):c.318+3A>T	rs746765533	0.00002
NM_001077350.3(NPRL3):c.905C>T (p.Ala302Val)	rs777790535	0.00002

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