Variants with conflicting interpretations "established risk allele" and "association"

Submission 1 (established risk allele) minimum review status:		Submission 1 (established risk allele) method:
Submission 2 (association) minimum review status:		Submission 2 (association) 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_001379610.1(SPINK1):c.101A>G (p.Asn34Ser)	rs17107315	0.00797
NM_000038.6(APC):c.3920T>A (p.Ile1307Lys)	rs1801155	0.00116

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