List of variants in gene DBT reported as benign by Illumina Laboratory Services, Illumina

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: 29

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HGVS	dbSNP	gnomAD frequency
NM_001918.5(DBT):c.*5546G>A	rs11166412	0.78278
NM_001918.5(DBT):c.*3233C>T	rs2784174	0.74803
NM_001918.5(DBT):c.*5150A>G	rs6701655	0.74788
NM_001918.5(DBT):c.*6228A>T	rs4281338	0.74605
NM_001918.5(DBT):c.1210-9A>T	rs34229137	0.31080
NM_001918.5(DBT):c.*5317T>C	rs11166413	0.30273
NM_001918.5(DBT):c.*6903T>A	rs10783125	0.12973
NM_001918.5(DBT):c.*9082C>T	rs72728160	0.12046
NM_001918.5(DBT):c.1210-10T>A	rs183058253	0.04736
NM_001918.5(DBT):c.*4395G>A	rs79471979	0.04616
NM_001918.5(DBT):c.*985C>T	rs11166414	0.04442
NM_001918.5(DBT):c.*5838G>A	rs79887429	0.04380
NM_001918.5(DBT):c.715A>G (p.Ile239Val)	rs72973763	0.03442
NM_001918.5(DBT):c.*6646G>T	rs72973747	0.03031
NM_001918.5(DBT):c.*344G>T	rs58607634	0.02661
NM_001918.5(DBT):c.*8977T>C	rs113536022	0.02409
NM_001918.5(DBT):c.*4872A>G	rs12044663	0.02047
NM_001918.5(DBT):c.*470G>A	rs148424011	0.01941
NM_001918.5(DBT):c.*5919A>G	rs115442245	0.01236
NM_001918.5(DBT):c.1281+6T>G	rs140115881	0.01022
NM_001918.5(DBT):c.724T>C (p.Ser242Pro)	rs146249007	0.00864
NM_001918.5(DBT):c.*7358C>T	rs143822588	0.00725
NM_001918.5(DBT):c.*8944A>G	rs77587629	0.00713
NM_001918.5(DBT):c.*4094C>A	rs74825164	0.00603
NM_001918.5(DBT):c.506G>A (p.Arg169Gln)	rs34267966	0.00341
NM_001918.5(DBT):c.*2810A>G	rs116578353	0.00337
NM_001918.5(DBT):c.*5347C>T	rs116806523	0.00337
NM_001918.5(DBT):c.*594A>G	rs147781191	0.00150
NM_001918.5(DBT):c.*4506A>G	rs112901689	0.00064

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