ClinVar Miner

List of variants reported as uncertain significance for Hyperinsulinemic hypoglycemia, familial, 1; Diabetes mellitus, permanent neonatal 3 by New York Genome Center

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000352.6(ABCC8):c.823-8C>T	rs201000679	0.00014
NM_000352.6(ABCC8):c.2164C>T (p.Leu722Phe)
NM_000352.6(ABCC8):c.343A>G (p.Met115Val)	rs146695489

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