Variants in gene POLR3A with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status:		Submission 1 (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: 3

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HGVS	dbSNP	gnomAD frequency
NM_007055.4(POLR3A):c.927C>T (p.Asp309=)	rs41274610	0.00287
NM_007055.4(POLR3A):c.1771-5del	rs544204280
NM_007055.4(POLR3A):c.1771-6C>A	rs115020338

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