List of variants in gene HADH reported as benign for Hyperinsulinemic 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)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_005327.7(HADH):c.710-845C>G	rs201019894	0.00057
NM_005327.7(HADH):c.133-15C>T	rs190144364	0.00013
NM_005327.7(HADH):c.-34C>T	rs748286204	0.00009
NM_005327.7(HADH):c.291G>T (p.Leu97=)	rs552317372	0.00007
NM_005327.7(HADH):c.132+7G>T	rs534966818	0.00005
NM_005327.7(HADH):c.324C>T (p.Ser108=)	rs373153417	0.00004
NM_005327.7(HADH):c.384C>T (p.Asn128=)	rs369550874	0.00004
NM_005327.7(HADH):c.795C>T (p.Val265=)	rs143416676	0.00004
NM_005327.7(HADH):c.486A>G (p.Arg162=)	rs377521547	0.00003
NM_005327.7(HADH):c.159A>G (p.Val53=)	rs148846625	0.00001
NM_005327.7(HADH):c.579A>G (p.Thr193=)	rs762771153	0.00001
NM_005327.7(HADH):c.264C>T (p.Ala88=)	rs201324954

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