ClinVar Miner

List of variants reported as likely benign for Hyperinsulinemic hypoglycemia, familial, 1 by Counsyl

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000352.6(ABCC8):c.1678G>A (p.Val560Met)	rs4148619	0.00019
NM_000352.6(ABCC8):c.2256-16del	rs774508952
NM_000352.6(ABCC8):c.2475+19G>A	rs373894772

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