ClinVar Miner

Variants with conflicting interpretations "likely pathogenic" and "association not found"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (association not found) minimum review status:		Submission 2 (association not found) method:
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 2

HGVS	dbSNP	gnomAD frequency
NM_000512.5(GALNS):c.1365-2A>G
NM_000512.5(GALNS):c.423-1G>A	rs2143002474

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