ClinVar Miner

Variants with conflicting interpretations "likely pathogenic" from KTest Genetics, KTest and "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: 1
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HGVS dbSNP gnomAD frequency
NM_005159.5(ACTC1):c.941G>A (p.Arg314His) rs121912673 0.00003

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