ClinVar Miner

List of variants in gene combination GOSR2, LRRC37A2 reported as likely pathogenic for Unverricht-Lundborg syndrome

Included ClinVar conditions (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)
		ClinVar version:

Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NM_004287.5(GOSR2):c.337-2A>G	rs1568177307

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