ClinVar Miner

Variants in gene DAG1 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 8
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HGVS dbSNP gnomAD frequency
NM_004393.6(DAG1):c.2256C>T (p.His752=) rs1801143 0.30176
NM_004393.6(DAG1):c.259A>G (p.Ile87Val) rs116717961 0.00640
NM_004393.6(DAG1):c.258G>C (p.Leu86Phe) rs145403829 0.00314
NM_004393.6(DAG1):c.599C>G (p.Thr200Ser) rs41290704 0.00167
NM_004393.6(DAG1):c.331G>A (p.Asp111Asn) rs117209107 0.00072
NM_004393.6(DAG1):c.286-10del rs747305463 0.00012
NM_004393.6(DAG1):c.-116-4dup rs200455639
NM_004393.6(DAG1):c.384G>T (p.Val128=) rs143829263

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