ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 15
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HGVS dbSNP gnomAD frequency
NM_001918.5(DBT):c.*8983dup rs67820832 0.02408
NM_001918.5(DBT):c.*8607G>A rs150241889 0.01296
NM_001918.5(DBT):c.*8552A>T rs543411196 0.00862
NM_001918.5(DBT):c.1418A>G (p.Asn473Ser) rs75525811 0.00196
NM_001918.5(DBT):c.*4273C>A rs12568926 0.00074
NM_001918.5(DBT):c.*5969C>T rs141483625 0.00055
NM_001918.5(DBT):c.*7307G>C rs182980145 0.00051
NM_001918.5(DBT):c.1210-11T>A rs751951997 0.00049
NM_001918.5(DBT):c.*6716C>G rs529415312 0.00033
NM_001918.5(DBT):c.*7698C>T rs185528579 0.00024
NM_001918.5(DBT):c.1210-8A>T rs535837017 0.00023
NM_001918.5(DBT):c.747C>A (p.Gly249=) rs200612682 0.00013
NM_001918.5(DBT):c.*2619G>A rs541064624
NM_001918.5(DBT):c.*2633AAAT[7] rs773873766
NM_001918.5(DBT):c.*3869del rs141830881

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