ClinVar Miner

Variants in gene DBT with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status: Submission 2 (uncertain significance) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 4
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NM_001918.4(DBT):c.198G>A (p.Gln66=)
NM_001918.4(DBT):c.291C>T (p.Ser97=) rs201318480
NM_001918.4(DBT):c.327C>T (p.Thr109=) rs138796800
NM_001918.4(DBT):c.753C>T (p.Asp251=) rs79292123

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