List of variants in gene DBT reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_001918.5(DBT):c.1281+31T>G	rs115696850	0.03046
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.1418A>G (p.Asn473Ser)	rs75525811	0.00196
NM_001918.5(DBT):c.327C>T (p.Thr109=)	rs138796800	0.00078
NM_001918.5(DBT):c.318T>G (p.Ala106=)	rs146259768	0.00011
NM_001918.5(DBT):c.1281+5A>G	rs199571242	0.00006
NM_001918.5(DBT):c.1143C>G (p.Gly381=)	rs1052326198	0.00004
NM_001918.5(DBT):c.231A>G (p.Arg77=)	rs1028461413	0.00001
NM_001918.5(DBT):c.1282-13T>A	rs1374973220
NM_001918.5(DBT):c.1282-14T>A	rs1315625069
NM_001918.5(DBT):c.1282-14_1282-9del	rs760164623
NM_001918.5(DBT):c.1282-15T>A	rs763988935
NM_001918.5(DBT):c.1282-16T>A
NM_001918.5(DBT):c.1282-8A>C
NM_001918.5(DBT):c.251+19dup	rs201469612

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