Variants in gene combination ENG, LOC102723566 with conflicting interpretations reported as "benign and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001114753.3(ENG):c.1374A>G (p.Pro458=)	rs34828244	0.00879
NM_001114753.3(ENG):c.1452C>T (p.Ser484=)	rs115450389	0.00311
NM_001114753.3(ENG):c.1510G>A (p.Val504Met)	rs116330805	0.00311
NM_001114753.3(ENG):c.1407G>A (p.Pro469=)	rs41302657	0.00048
NM_001114753.3(ENG):c.1455G>A (p.Glu485=)	rs150456852	0.00046
NM_001114753.3(ENG):c.1633G>A (p.Gly545Ser)	rs142896669	0.00037
NM_001114753.3(ENG):c.1533G>A (p.Ala511=)	rs140760635	0.00027
NM_001114753.3(ENG):c.1686+6T>G	rs369766351	0.00019
NM_001114753.3(ENG):c.1135-7G>A	rs201359896	0.00008

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