ClinVar Miner

Variants in gene MERTK 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: 2
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NM_006343.3(MERTK):c.2593C>T (p.Arg865Trp) rs2230516
NM_006343.3(MERTK):c.2851G>A (p.Ala951Thr) rs148261231

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