List of variants in gene ACADSB reported as pathogenic for not provided

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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001609.4(ACADSB):c.303+1G>A	rs147936696	0.00036
NM_001609.4(ACADSB):c.1159G>A (p.Glu387Lys)	rs188094280	0.00029
NM_001609.4(ACADSB):c.1165A>G (p.Met389Val)	rs201877440	0.00004
NM_001609.4(ACADSB):c.295C>T (p.Gln99Ter)	rs760791287	0.00001
NM_001609.4(ACADSB):c.303+3A>G	rs1345480688	0.00001

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