Variants with conflicting interpretations "association" and "likely pathogenic"

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

Total variants with conflicting interpretations: 7

HGVS	dbSNP	gnomAD frequency
NM_002386.4(MC1R):c.880G>C (p.Asp294His)	rs1805009	0.01121
NM_001379610.1(SPINK1):c.101A>G (p.Asn34Ser)	rs17107315	0.00797
NM_007272.3(CTRC):c.760C>T (p.Arg254Trp)	rs121909293	0.00386
NM_006361.6(HOXB13):c.251G>A (p.Gly84Glu)	rs138213197	0.00160
NM_000038.6(APC):c.3920T>A (p.Ile1307Lys)	rs1801155	0.00116
NM_005157.6(ABL1):c.944C>T (p.Thr315Ile)	rs121913459
Single allele

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