List of variants in gene DBT reported as benign for not specified

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: 17

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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.1210-9A>T	rs34229137	0.31080
NM_001918.5(DBT):c.1210-10T>A	rs183058253	0.04736
NM_001918.5(DBT):c.715A>G (p.Ile239Val)	rs72973763	0.03442
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.506G>A (p.Arg169Gln)	rs34267966	0.00341
NM_001918.5(DBT):c.76T>C (p.Cys26Arg)	rs145674833	0.00302
NM_001918.5(DBT):c.753C>T (p.Asp251=)	rs79292123	0.00179
NM_001918.5(DBT):c.175+37G>A	rs76902654	0.00154
NM_001918.5(DBT):c.327C>T (p.Thr109=)	rs138796800	0.00078
NM_001918.5(DBT):c.1210-9_1210-8insT	rs201755806	0.00020
NM_001918.5(DBT):c.1210-10_1210-9del	rs794726986	0.00004
NM_001918.5(DBT):c.1210-10del	rs398123658
NM_001918.5(DBT):c.1210-4del	rs201117345
NM_001918.5(DBT):c.1282-14_1282-10del	rs752915898
NM_001918.5(DBT):c.251+19dup	rs201469612

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