Variants in gene combination ABCA12, SNHG31 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_173076.3(ABCA12):c.6919A>G (p.Ile2307Val)	rs150196545	0.00105
NM_173076.3(ABCA12):c.6704A>C (p.Glu2235Ala)	rs138504099	0.00043

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