ClinVar Miner

Variants with conflicting interpretations "likely benign" and "likely benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Show significances as they were submitted (without aggregation into standard terms)

Total variants with conflicting interpretations: 1

HGVS	dbSNP	gnomAD frequency
GRCh38/hg38 7q11.1-11.21(chr7:61006478-62410831)x1

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