Variants in gene combination ASTN2, TRIM32 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_012210.4(TRIM32):c.1254G>A (p.Val418=)	rs1661300	0.10569
NM_012210.4(TRIM32):c.770C>G (p.Thr257Arg)	rs3747834	0.00017

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