ClinVar Miner

Variants in gene WDR19 with conflicting interpretations "uncertain significance" and "likely benign"

Submission 1 (uncertain significance) minimum review status: Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 4
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HGVS dbSNP
NM_025132.4(WDR19):c.2671C>T (p.His891Tyr) rs200266424
NM_025132.4(WDR19):c.2715G>A (p.Lys905=) rs200339331
NM_025132.4(WDR19):c.2792A>C (p.Tyr931Ser) rs187546086
NM_025132.4(WDR19):c.3008A>G (p.Glu1003Gly) rs201354264

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