Variants in gene combination ARID1A, LOC129929837 with conflicting interpretations reported as "uncertain significance and "likely benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_006015.6(ARID1A):c.945C>T (p.Asp315=)	rs2080280639	0.00001
NM_006015.6(ARID1A):c.1029_1040dup (p.Ala349_Ser350insAlaAlaAlaAla)	rs997979656
NM_006015.6(ARID1A):c.670C>G (p.Pro224Ala)	rs1057520224
NM_006015.6(ARID1A):c.729GGC[4] (p.Ala247dup)	rs749970078

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