ClinVar Miner

List of variants in gene combination ABCC8, LOC110121471 reported as likely benign for Leucine-induced hypoglycemia

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_000352.6(ABCC8):c.2390+123C>T	rs4148631	0.71455
NM_000352.6(ABCC8):c.2390+93C>T	rs4148630	0.71434

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