ClinVar Miner

Variants with conflicting interpretations "pathogenic" from KTest Genetics, KTest and "likely pathogenic" from any submitter

Minimum review status of the submission from KTest Genetics, KTest: Collection method of the submission from KTest Genetics, KTest:
Minimum review status of the other submission: Collection method of the other submission:
ClinVar version:
Total variants with conflicting interpretations: 3
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HGVS dbSNP gnomAD frequency
NM_001134363.3(RBM20):c.1907G>A (p.Arg636His) rs267607004 0.00001
NM_001276345.2(TNNT2):c.548G>A (p.Arg183Gln) rs397516471
NM_001276345.2(TNNT2):c.650AGA[3] (p.Lys220del) rs45578238

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