List of variants in gene HADHB reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000183.3(HADHB):c.397A>G (p.Thr133Ala)	rs371159065	0.00006
NM_000183.3(HADHB):c.589T>C (p.Ser197Pro)	rs142475516	0.00002
NM_000183.3(HADHB):c.111T>C (p.Ala37=)	rs1574650470
NM_000183.3(HADHB):c.1154A>C (p.Gln385Pro)	rs1574669267
NM_000183.3(HADHB):c.154A>T (p.Arg52Trp)
NM_000183.3(HADHB):c.446T>C (p.Val149Ala)
NM_000183.3(HADHB):c.487G>A (p.Gly163Ser)	rs1574662730
NM_000183.3(HADHB):c.563dup (p.Ala189fs)	rs1064797251
NM_000183.3(HADHB):c.721C>G (p.Gln241Glu)	rs1574663511
NM_000183.3(HADHB):c.907G>A (p.Val303Met)

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