ClinVar Miner

Variants in gene DYRK1A 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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HGVS dbSNP
NM_001347721.2(DYRK1A):c.1509G>A (p.Ser503=) rs763907769
NM_001347721.2(DYRK1A):c.1803CCA[7] (p.His609_His610dup) rs760576043
NM_001347721.2(DYRK1A):c.208-28G>A rs552103257
NM_001347721.2(DYRK1A):c.300+7C>T rs537532878

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