ClinVar Miner

Variants with conflicting interpretations "pathogenic" from Research Group Niklas Dahl, Uppsala University and "likely pathogenic" from any submitter

Minimum review status of the submission from Research Group Niklas Dahl, Uppsala University: Collection method of the submission from Research Group Niklas Dahl, Uppsala University:
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_153700.2(STRC):c.4027C>T (p.Gln1343Ter) rs144948296 0.00018

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