List of variants in gene SLC46A1 reported as likely benign for anemia

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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_080669.6(SLC46A1):c.756C>G (p.Val252=)	rs185900287	0.00274
NM_080669.6(SLC46A1):c.642G>A (p.Leu214=)	rs145398587	0.00145
NM_080669.6(SLC46A1):c.294C>A (p.Leu98=)	rs371270310	0.00110
NM_080669.6(SLC46A1):c.906A>G (p.Lys302=)	rs572650603

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