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

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001114753.3(ENG):c.1510G>A (p.Val504Met)	rs116330805	0.00311
NM_001114753.3(ENG):c.1633G>A (p.Gly545Ser)	rs142896669	0.00037
NM_001114753.3(ENG):c.1447G>A (p.Val483Ile)	rs141330288	0.00034
NM_001114753.3(ENG):c.1258A>G (p.Met420Val)	rs143724056	0.00029
NM_001114753.3(ENG):c.1135-8C>T	rs79426098	0.00011
NM_001114753.3(ENG):c.1711C>T (p.Arg571Cys)	rs764262721	0.00005
NM_001114753.3(ENG):c.1389C>T (p.Ala463=)	rs200168633	0.00004
NM_001114753.3(ENG):c.1572C>T (p.Pro524=)	rs760682477	0.00002
NM_001114753.3(ENG):c.1273-5C>T	rs779103881	0.00001
NM_001114753.3(ENG):c.1216C>G (p.Arg406Gly)	rs751787590
NM_001114753.3(ENG):c.1429-8C>G	rs376169815

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