List of variants in gene HADH reported as uncertain risk allele for Hyperinsulinemic hypoglycemia

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_005327.7(HADH):c.881A>G (p.Asn294Ser)	rs36030668	0.00738
NM_005327.7(HADH):c.643C>A (p.Pro215Thr)	rs140413151	0.00198
NM_005327.7(HADH):c.614G>C (p.Gly205Ala)	rs144699575	0.00079
NM_005327.7(HADH):c.809C>T (p.Thr270Met)	rs577954688	0.00017
NM_005327.7(HADH):c.361G>A (p.Val121Met)	rs377615662	0.00006
NM_005327.7(HADH):c.47C>T (p.Ser16Phe)	rs374248298	0.00003
NM_005327.7(HADH):c.479C>T (p.Thr160Ile)	rs780252799	0.00002
NM_005327.7(HADH):c.171C>A (p.Asp57Glu)	rs137853102	0.00001
NM_005327.7(HADH):c.266G>A (p.Gly89Asp)	rs1292646768	0.00001
NM_005327.7(HADH):c.494G>A (p.Arg165Gln)	rs768880930	0.00001
NM_005327.7(HADH):c.823G>A (p.Asp275Asn)	rs150766162	0.00001
NM_005327.7(HADH):c.889G>A (p.Val297Ile)	rs376876153	0.00001
NM_005327.7(HADH):c.740C>T (p.Ala247Val)	rs1736337431

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