Variants with conflicting interpretations "affects" and "association"

Submission 1 (affects) minimum review status:		Submission 1 (affects) 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: 3

HGVS	dbSNP	gnomAD frequency
NM_004827.3(ABCG2):c.34G>A (p.Val12Met)	rs2231137	0.07216
NM_002386.4(MC1R):c.478C>T (p.Arg160Trp)	rs1805008	0.04851
NM_002386.4(MC1R):c.451C>T (p.Arg151Cys)	rs1805007	0.04832

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