Variants in gene SLC17A5 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (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: 7

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HGVS	dbSNP	gnomAD frequency
NM_012434.5(SLC17A5):c.246G>A (p.Ala82=)	rs472294	0.10691
NM_012434.5(SLC17A5):c.1111+7G>A	rs146729568	0.01982
NM_012434.5(SLC17A5):c.886G>A (p.Val296Ile)	rs16883930	0.01342
NM_012434.5(SLC17A5):c.820-3C>T	rs12201641	0.00436
NM_012434.5(SLC17A5):c.553A>G (p.Met185Val)	rs34348416	0.00257
NM_012434.5(SLC17A5):c.1324G>A (p.Val442Ile)	rs74360232	0.00215
NM_012434.5(SLC17A5):c.957C>A (p.Ile319=)	rs147732875	0.00041

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