ClinVar Miner

Variants with conflicting interpretations "uncertain significance" from ISCA site 15 and "likely benign" from any submitter

Minimum review status of the submission from ISCA site 15:		Collection method of the submission from ISCA site 15:
Minimum review status of the other submission:		Collection method of the other submission:
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 1

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HGVS	dbSNP	gnomAD frequency
GRCh38/hg38 7q11.1-11.21(chr7:61006478-62410831)x3

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