Variants in gene MMP21 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 3

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HGVS	dbSNP	gnomAD frequency
NM_147191.1(MMP21):c.1046A>G (p.Glu349Gly)	rs28381302	0.00331
NM_147191.1(MMP21):c.558C>T (p.Ser186=)	rs373268684	0.00158
NM_147191.1(MMP21):c.732G>C (p.Gly244=)	rs28381292	0.00024

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