List of variants in gene DBT reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001918.5(DBT):c.1150A>G (p.Ser384Gly)	rs12021720	0.87100
NM_001918.5(DBT):c.724T>C (p.Ser242Pro)	rs146249007	0.00864
NM_001918.5(DBT):c.1282-13_1282-9del	rs761681999	0.00456
NM_001918.5(DBT):c.1210-10del	rs398123658
NM_001918.5(DBT):c.1210-4del	rs201117345
NM_001918.5(DBT):c.1282-14_1282-9del	rs760164623
NM_001918.5(DBT):c.251+19dup	rs201469612

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