ClinVar Miner

Variants in gene combination KLLN, PTEN with conflicting interpretations reported as "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: 5
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HGVS dbSNP
NM_000314.6(PTEN):c.-1059C>G rs144620057
NM_001126049.2(KLLN):c.-671A>G rs70937047
NM_001126049.2(KLLN):c.-840G>A rs563841270
NM_001126049.2(KLLN):c.-898G>A rs538728843
NM_001126049.2(KLLN):c.-955G>T rs587781128

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