Variants with conflicting interpretations "risk factor" and "affects"

Submission 1 (risk factor) minimum review status:		Submission 1 (risk factor) method:
Submission 2 (affects) minimum review status:		Submission 2 (affects) method:
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 4

HGVS	dbSNP	gnomAD frequency
NM_002087.4(GRN):c.*78C>T	rs5848	0.41298
NM_016945.3(TAS2R16):c.516T>G (p.Asn172Lys)	rs846664	0.08801
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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