Variants with conflicting interpretations "likely benign" from PreventionGenetics, part of Exact Sciences and "association" from any submitter

Minimum review status of the submission from PreventionGenetics, part of Exact Sciences:		Collection method of the submission from PreventionGenetics, part of Exact Sciences:
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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 5

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HGVS	dbSNP	gnomAD frequency
NM_001902.6(CTH):c.1208G>T (p.Ser403Ile)	rs1021737	0.23572
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.880G>C (p.Asp294His)	rs1805009	0.01121
NM_006949.4(STXBP2):c.1586G>C (p.Arg529Pro)	rs35490401

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