ClinVar Miner

List of variants reported as likely benign for diabetes mellitus, permanent neonatal 3 by Pars Genome Lab

Included ClinVar conditions (4):

Diabetes mellitus, permanent neonatal 3
Diabetes mellitus, transient neonatal, 2; Hyperinsulinemic hypoglycemia, familial, 1; Leucine-induced hypoglycemia; Type 2 diabetes mellitus; Diabetes mellitus, permanent neonatal 3
Hyperinsulinemic hypoglycemia, familial, 1; Diabetes mellitus, permanent neonatal 3
Hyperinsulinemic hypoglycemia, familial, 1; Leucine-induced hypoglycemia; Diabetes mellitus, permanent neonatal 3

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Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000352.6(ABCC8):c.2390+123C>T	rs4148631	0.70926
NM_000352.6(ABCC8):c.2390+93C>T	rs4148630	0.70902
NM_000352.6(ABCC8):c.4119+93G>T	rs4148644	0.21307

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