ClinVar Miner

Variants with conflicting interpretations "risk factor" and "pathogenic, low penetrance"

Submission 1 (risk factor) minimum review status:		Submission 1 (risk factor) method:
Submission 2 (pathogenic, low penetrance) minimum review status:		Submission 2 (pathogenic, low penetrance) 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_000506.5(F2):c.*97G>A	rs1799963	0.00979
NM_000350.3(ABCA4):c.5882G>A (p.Gly1961Glu)	rs1800553	0.00269

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