ClinVar Miner

Variants in gene MERTK with conflicting interpretations "uncertain significance" and "benign"

Submission 1 (uncertain significance) minimum review status: Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 6
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HGVS dbSNP
NM_006343.3(MERTK):c.1261C>T (p.Arg421Trp) rs142985827
NM_006343.3(MERTK):c.1340G>A (p.Arg447Gln)
NM_006343.3(MERTK):c.2079+10del rs529766238
NM_006343.3(MERTK):c.2593C>T (p.Arg865Trp) rs2230516
NM_006343.3(MERTK):c.773C>A (p.Ala258Glu) rs35252762
NM_006343.3(MERTK):c.960+9C>A rs373198570

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