List of variants in gene SLC11A1 reported as benign for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_000578.4(SLC11A1):c.1328T>C (p.Val443Ala)	rs17215556	0.00708
NM_000578.4(SLC11A1):c.501-4T>G	rs17221980	0.00498
NM_000578.4(SLC11A1):c.522C>T (p.Val174=)	rs139234551	0.00192
NM_000578.4(SLC11A1):c.1165-7A>C	rs17221987	0.00141
NM_000578.4(SLC11A1):c.1492G>A (p.Gly498Ser)	rs142636978	0.00141
NM_000578.4(SLC11A1):c.1450G>C (p.Val484Leu)	rs138316650

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