ClinVar Miner

Variants in gene TK2 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 5
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HGVS dbSNP
NM_004614.5(TK2):c.156+15T>C rs80083556
NM_004614.5(TK2):c.157-12G>A rs117229729
NM_004614.5(TK2):c.231+10C>T rs187517309
NM_004614.5(TK2):c.700-13G>A rs16956600
NM_004614.5(TK2):c.94C>T (p.Arg32Trp) rs200121712

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